Acetic Anhydride → HCID 11770291, 화합물

HRID 1272509노트

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HRID 1272509 반응식
[Cl-].[Al+3].[Cl-].[Cl-].[C:5](OC(=O)C)(=[O:7])[CH3:6].[CH2:12]([O:14][C:15]([C:17]1[NH:18][C:19]2[C:24]([CH:25]=1)=[CH:23][CH:22]=[CH:21][CH:20]=2)=[O:16])[CH3:13]>ClC(Cl)C>[CH2:12]([O:14][C:15]([C:17]1[NH:18][C:19]2[C:24]([C:25]=1[C:5](=[O:7])[CH3:6])=[CH:23][CH:22]=[CH:21][CH:20]=2)=[O:16])[CH3:13].[CH2:12]([O:14][C:15]([C:17]1[NH:18][C:19]2[C:24]([CH:25]=1)=[CH:23][C:22]([C:5](=[O:7])[CH3:6])=[CH:21][CH:20]=2)=[O:16])[CH3:13]

참가 물질

6

반응물 3

HCID 7918Acetic AnhydrideHCID 73125Ethyl indole-2-carboxylateHCID 6451240Aluminum(III) Chloride

생성물 2

HCID 4162576HCID 4162576, 화합물수율 13%HCID 11770291HCID 11770291, 화합물수율 52%

시약·촉매·용매 1

HCID 63651,1-Dichloroethane용매2회

반응 조건

온도
40 °C

실험 절차

Aluminum chloride (7.75 g, 0.058 mol) was suspended in 200 ml of anhydrous dichloroethane at room temp. followed by a slow addition of acetic anhydride (2.74 mL, 0.03 mol). The mixture was stirred at room temp for 10 minutes after which, 1H-indole-2-carboxylic acid ethyl ester (1b, 5.0 g, 0.0264 mol) was added as a solution in 15 mL of dichloroethane. The reaction mixture was stirred under nitrogen at 40° C. for 10 h. The reaction was quenched with an ice-water mixture and the organic layer was washed with water (3×). The organic phase was dried over anh. Na2SO4, filtered and concentrated in vacuo. Chromatography on SiO2 (4% Ethyl acetate/96% CH2Cl2) provided 3.2 g of 3-acetyl-1H-indole-2-carboxylic acid ethyl ester 2b (52%) and 770 mg of 5-acetyl-1H-indole-2-carboxylic acid ethyl ester 3b (13%).

후처리

  1. customThe reaction was quenched with an ice-water mixture
  2. washthe organic layer was washed with water (3×)
  3. dry with materialThe organic phase was dried over anh. Na2SO4
  4. filtrationfiltered
  5. concentrationconcentrated in vacuo

출처 및 근거

ORD 기록
ord-2678447afd6f4fb9b2ecd6081fe235e3
출처 데이터셋
uspto-grants-2007_04
특허 번호
US07208600B2

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