Tag: M.W:100-200

20197-75-5, Methyl 1,4-Benzodioxan-6-carboxylate is a benzodioxans compound, ?involved in a variety of chemical synthesis. Rlated chemical reaction is continuously updated

A stirred solution of compound 3 (0.1 mol) in ethanol (50 mL) was treated with the hydrazine hydrate (85%), under 90 oC for 5 d. The sovlent was removed leaving oil which was dissovled in ethyl acetate (20 ml) and extracted with water (40 ml). After drying the organic layer with anhydrous Na2SO4 and evaporating the solvent under reduced pressure a solid appeared. The solid was recyrstallized from ethanol to obtain the compound 6.

20197-75-5, 20197-75-5 Methyl 1,4-Benzodioxan-6-carboxylate 3802178, abenzodioxans compound, is more and more widely used in various fields.

Reference£º
Article; Sun, Juan; Li, Ming-Hui; Qian, Shao-Song; Guo, Feng-Jiao; Dang, Xiao-Fang; Wang, Xiao-Ming; Xue, Ya-Rong; Zhu, Hai-Liang; Bioorganic and Medicinal Chemistry Letters; vol. 23; 10; (2013); p. 2876 – 2879;,
Benzodioxan
1,4-Benzodioxane | C8H8O2 – PubChem

With the rapid development and complex challenges of chemical substances, new drug synthesis pathways are usually the most effective.2879-20-1,1-(2,3-Dihydrobenzo[b][1,4]dioxin-6-yl)ethanone,as a common compound, the synthetic route is as follows.,2879-20-1

General procedure: Equimolar quantities of substituted benzaldehyde and 1-(2H-1,3-benzodioxol-5-yl)ethan-1-one or 1-(2,3-dihydro-1,4-benzodioxin-6-yl)ethan-1-one were dissolved in 40% KOH and ethanol. The reactionmixture was then stirred for 10 h and poured into ice-cold water. Theprecipitated product was washed with water, dried, and recrystallizedfrom ethanol.

The synthetic route of 2879-20-1 has been constantly updated, and we look forward to future research findings.

Reference£º
Article; Parambi, Della Grace Thomas; Oh, Jong Min; Baek, Seung Cheol; Lee, Jae Pil; Tondo, Anna Rita; Nicolotti, Orazio; Kim, Hoon; Mathew, Bijo; Bioorganic Chemistry; vol. 93; (2019);,
Benzodioxan
1,4-Benzodioxane | C8H8O2 – PubChem

With the rapid development and complex challenges of chemical substances, new drug synthesis pathways are usually the most effective.2879-20-1,1-(2,3-Dihydrobenzo[b][1,4]dioxin-6-yl)ethanone,as a common compound, the synthetic route is as follows.

General procedure: To 1-(2,3-dihydrobenzo[b][1,4]dioxin-6-yl)ethan-1-one(A) (1 mmol) alcohol solution (5 mL) was added substituted benzaldehyde(1 mmol). After dissolution, 50% NaOH (0.5 mL) was added. After confirming the completion of the reaction by thin layer chromatography, the sediment was filtered, washed with ethanol and dried to obtain chalcone

2879-20-1, As the paragraph descriping shows that 2879-20-1 is playing an increasingly important role.

Reference£º
Article; Yang, Yu-Shun; Yang, Bing; Zou, Yan; Li, Guigen; Zhu, Hai-Liang; Bioorganic and Medicinal Chemistry; vol. 24; 13; (2016); p. 3052 – 3061;,
Benzodioxan
1,4-Benzodioxane | C8H8O2 – PubChem

3663-80-7, 2,3-Dihydrobenzo[b][1,4]dioxine-2-carboxylic acid is a benzodioxans compound, ?involved in a variety of chemical synthesis. Rlated chemical reaction is continuously updated

EXAMPLE 22 Preparation of (-)-N-[[3-[4-[4-[(2,3-Dihydro-1,4-benzodioxin-2-yl)carbonyl]-1-piperazinyl]-3-fluorophenyl]-4,5-dihydro-5-isoxazolyl]methyl]acetamide. To a flame dried flask containing (-)-N-[[4,5-dihydro-3-[3-fluoro-4-(1-piperazinyl)phenyl]-5-isoxazolyl]methyl]acetamide (Step 1, Example 21) (200 mg), 1,4-benzodioxan-2-carboxylic acid (135 mg), DMAP (9 mg) in pyridine (7 mL) is added EDC (144 mg) at ambient temperature and stirred for 48 hours. The reaction is diluted with CH2Cl2 (25 mL) and washed with H2O (2 X 50 mL) and saline (50 mL). The organic phase is dried over sodium sulfate, concentrated in vacuo and chromatographed on silica gel (230-400 mesh), eluding with chloroform/methanol (99/1). The appropriate fractions are combined (Rf= 0.29,TLC, chloroform/methanol, 95/5), concentrated to give the title compound, mp 158-161 ¡ãC, [alpha]25D -43¡ã (CHCl3)., 3663-80-7

The synthetic route of 3663-80-7 has been constantly updated, and we look forward to future research findings.

Reference£º
Patent; PHARMACIA & UPJOHN COMPANY; EP1054874; (2002); B1;,
Benzodioxan
1,4-Benzodioxane | C8H8O2 – PubChem

With the rapid development and complex challenges of chemical substances, new drug synthesis pathways are usually the most effective.2879-20-1,1-(2,3-Dihydrobenzo[b][1,4]dioxin-6-yl)ethanone,as a common compound, the synthetic route is as follows.,2879-20-1

General procedure: 3.3. Reaction procedure for the synthesis of 5a The reaction was conducted in a 10 mL of V-type ask equippedwith triangle magnetic stirring. In a typical reaction, 1a(0.20 mmol) was mixed with 2a (0.20 mmol) and 4a (0.20 mmol)and BF3Et2O (50 mol %) in nitromethane (1.0 mL). The mixturewas then stirred at 80 Cforve hours. After reaction, 5a wasobtained by isolation with preparative TLC (eluting solution: pe-troleum ether/ethyl acetate5/1 (v/v)) in 77% (0.15 mmol, 51.1 mg)yield.

The synthetic route of 2879-20-1 has been constantly updated, and we look forward to future research findings.

Reference£º
Article; Wang, Man; Liu, Changhui; Gu, Yanlong; Tetrahedron; vol. 72; 43; (2016); p. 6854 – 6865;,
Benzodioxan
1,4-Benzodioxane | C8H8O2 – PubChem

With the rapid development and complex challenges of chemical substances, new drug synthesis pathways are usually the most effective.4442-53-9,2,3-Dihydrobenzo[b][1,4]dioxine-5-carboxylic acid,as a common compound, the synthetic route is as follows.,4442-53-9

Intermediate 35: 2-diazo-1-(2,3-dihvdro-1 ,4-benzodioxin-5-yl)ethanone; A solution of 1 g of 2,3-dihydro-1 ,4-benzodioxin-5-carboxylic acid (5.55 mmole, Aldrich) in 30.7 mL of SOCI2 was stirred at 850C for 1 h in a dry flask under nitrogen atmosphere. The excess of SOCI2 was removed under reduced pressure, the resulting crude oil was dissolved in 20.3 ml. of MeCN and to this solution, a solution of TMSCHN2 2M in hexane (11.1 mmole, Aldrich) was added dropwise at O0C. The reaction mixture was warmed to RT and stirred for 2 h. A 1 M solution of citric acid was added and then extracted with AcOEt. The organic layer was washed with a saturated solution of NaHCC>3, dried over Na2SO4 and concentrated under reduced pressure. The crude oil was purified by flash chromatography (from CH to CH/AcOEt 80/20) to give the title compound as a yellow oil (489 mg, 42percent). 1H-NMR (500 MHz, CDCI3): delta 4.29-4.34 (2H, m), 4.35-4.40 (2H, m), 6.25 (1 H, s), 6.92 (1 H, t), 7.02 (1 H, dd), 7.46 (1 H, s); m/z (ES): 205 [M+H]+.

As the paragraph descriping shows that 4442-53-9 is playing an increasingly important role.

Reference£º
Patent; GLAXO GROUP LIMITED; WO2008/148853; (2008); A1;,
Benzodioxan
1,4-Benzodioxane | C8H8O2 – PubChem

4442-53-9, 2,3-Dihydrobenzo[b][1,4]dioxine-5-carboxylic acid is a benzodioxans compound, ?involved in a variety of chemical synthesis. Rlated chemical reaction is continuously updated,4442-53-9

7-chlorosulfonyl-1,4-benzodioxane-5-carboxylic acid 670 g of chlorosulfonic acid were introduced into a balloon flask provided with a condenser and a thermometer. 173 g of 1,4-benzodioxane-5-carboxylic acid were added in portions with the temperature being maintained at 5¡ã-10¡ã C. The mixture was heated at 55¡ã C. and then cooled and poured into ice. The precipitate was dried off, washed and dried again. 250 g of 7-chlorosulfonyl-1,4-benzodioxane-5-carboxylic acid were obtained (M.P.: 210¡ã-215¡ã C.; yield: 93.5percent).

As the paragraph descriping shows that 4442-53-9 is playing an increasingly important role.

Reference£º
Patent; Societe D’Etudes Scientifiques et Industrielles de L’ile-de-France; US4186135; (1980); A;,
Benzodioxan
1,4-Benzodioxane | C8H8O2 – PubChem

With the rapid development and complex challenges of chemical substances, new drug synthesis pathways are usually the most effective.3663-80-7,2,3-Dihydrobenzo[b][1,4]dioxine-2-carboxylic acid,as a common compound, the synthetic route is as follows.

To a solution of 2, 3-dihydrobenzo [b] [1, 4] dioxine-2-carboxylic acid (20.0 g, 111 mmol) in DCM (200 mL) was added oxalyl dichloride (30.0 g, 238 mmol) at 0 , followed by 0.5 ml of DMF. The solution was stirred at 0 for 1 hour, and at ambient temperature for 2h, and then concentrated to dryness. The resulting oil was diluted in THF (200 mL) . Malononitrile (11.0 g, 167 mmol) was added at 0 and followed by TEA (24.6 g, 167 mmol) . The final solution was stirred at ambient temperature for 16 h. The reaction mixture was filtered through a celite pad and the filtrate was added 200 mL of H2O, extracted with EA (200mL x 3) . The combined extracts were washed with brine (200mL x 3) , dried over sodium sulfate anhydrous and concentrated to get crude product (25.5 g) as brown oil, which was used in next step directly. MS: M/e 229 (M+1)+, 3663-80-7

As the paragraph descriping shows that 3663-80-7 is playing an increasingly important role.

Reference£º
Patent; BEIGENE, LTD.; ZHANG, Guoliang; REN, Bo; WANG, Hexiang; ZHAO, Haibo; GUO, Yunhang; WANG, Zhiwei; ZHOU, Changyou; (237 pag.)WO2016/8411; (2016); A1;,
Benzodioxan
1,4-Benzodioxane | C8H8O2 – PubChem

With the rapid development and complex challenges of chemical substances, new drug synthesis pathways are usually the most effective.31127-39-6,2,3-Dihydrobenzo[b][1,4]dioxine-6-carbaldehyde oxime,as a common compound, the synthetic route is as follows.,31127-39-6

General procedure: A solution of a respective oxime 2a,b or 5a,b (18 mmol) in acetic anhydride (10 mL) was heated to reflux for 8-12 h. Afterwards, the solvent was then removed in vacuo, the residue was quenched by adding cold water (10 mL), and keeping the temperature of the resulting mixture at 15-20C for 1-2 h. The formed precipitate was isolated, and dried at 40oC to give title compounds 3a,b or 6a,b, respectively.

The synthetic route of 31127-39-6 has been constantly updated, and we look forward to future research findings.

Reference£º
Article; Le-Nhat-Thuy, Giang; Dinh, Thuy Van; Pham-The, Hai; Nguyen Quang, Hung; Nguyen Thi, Nga; Dang Thi, Tuyet Anh; Hoang Thi, Phuong; Le Thi, Tu Anh; Nguyen, Ha Thanh; Nguyen Thanh, Phuong; Le Duc, Trung; Nguyen, Tuyen Van; Bioorganic and Medicinal Chemistry Letters; vol. 28; 23-24; (2018); p. 3741 – 3747;,
Benzodioxan
1,4-Benzodioxane | C8H8O2 – PubChem

With the rapid development and complex challenges of chemical substances, new drug synthesis pathways are usually the most effective.3663-80-7,2,3-Dihydrobenzo[b][1,4]dioxine-2-carboxylic acid,as a common compound, the synthetic route is as follows.,3663-80-7

Benzo-dioxane-2-carboxylic acid was added, 100 ml of absolute ethanol was added, and 10 ml of concentrated sulfuric acid was added, and the mixture was refluxed at 80 ¡ã C overnight (TLC). After the completion of the reaction, the reaction mixture was distilled under reduced pressure to one-fifth of its original volume, and 40 ml of water was added thereto. The mixture was extracted three times with ethyl acetate, washed with saturated NaHC03 solution and saturated NaCl solution, dried over MgS04 and distilled under reduced pressure to give The resulting ester, 2. Ommol, was dissolved in 30 ml of absolute ethanol and 2. l mmol of hydrazine hydrate 80 was added and refluxed overnight (TLC). Acetophenone (5.0 mmol) and benzaldehyde (5.1 mmol) were dissolved in 20 ml of ethanol, followed by magnetic separation. The resulting mixture was stirred at room temperature for 2 hours. After the completion of the reaction, the reaction mixture was distilled under reduced pressure until ethanol was distilled off. Stirring 10min to make the mixture hook, slowly dropping 40percent Na0H solution 10ml, magnetic stirring, room temperature reaction 2h (TLC detection reaction progress), the product of solid precipitation. After filtration, the solid was washed with a large amount of distilled water and finally washed three times with cold ethanol (3 ml each time) and dried. The product was mixed with ethanol and acetone (volume ratio of ethanol: acetone = 1: 1) The resulting hydrazide was dissolved in 25 ml of absolute ethanol and dissolved in 80 ¡ã C. The reaction was stirred at 80 ¡ã C for 20 h (TLC detection). After the completion of the reaction, the ethanol was evaporated to dryness under reduced pressure. The resulting mixture was subjected to column chromatography, and the first substance (raw material chalcone) was discarded using a developing solvent having a volume ratio of petroleum ether to ethyl acetate = 10: The mixed solution containing the second substance (target product) was distilled under reduced pressure to distill off the whole of the solvent to obtain the target product as a crude product, which was recrystallized from a mixture of ethanol and acetone (volume ratio of ethanol: acetone = 10: 1) The product (white crystals)

As the paragraph descriping shows that 3663-80-7 is playing an increasingly important role.

Reference£º
Patent; Nanjing University; Zhu, Hai Liang; Yang, yushun; Ding, Shu Ting; Zhang, Fei; Zhang, Yan Bin; Wang, Xiao Liang; Tang, Jian Feng; (22 pag.)CN103304546; (2016); B;,
Benzodioxan
1,4-Benzodioxane | C8H8O2 – PubChem