참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Acetic Anhydride | HCID 7918 | — |
| 반응물 | Aluminum(III) Chloride | HCID 6451240 | — |
| 반응물 | 1H-Indole-5-carboxylic acid, 1-(phenylsulfonyl)-, methyl ester | HCID 57517433 | — |
| 용매 | 1,1-Dichloroethane | HCID 6365 | — |
| 생성물 | 3-Acetyl-1-benzenesulfonylindole-5-carboxylic acid methyl ester | HCID 69890280 | 96% |
반응 단계
To a suspension of 10.7 g (80 mmol) of aluminum chloride in dichloroethane (80 ml) was added dropwise 4.83 g (40 mmol) of acetic anhydride. After stirring for 15 min, to the mixture was added dropwise 6.31 g (20 mmol) of the above-mentioned 1-benzenesulfonylindole-5-carboxylic acid methyl ester in dichloroethane (60 ml). After stirring for 2 hours at room temperature, to the mixture were added 5.33 g (40 mmol) of aluminum chloride and 2.04 g (20 mmol) of acetic anhydride. After stirring for 30 min, the mixture was poured into ice-water, extracted with ethyl acetate. The extract was washed twice with water, aqueous sodium bicarbonate and dried, and then concentrated. The obtained crystal was washed with isopropyl ether to give 6.82 g of 3-acetyl-1-benzenesulfonylindole-5-carboxylic acid methyl ester. Yield: 96%.
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US06333323B1 |
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| 출처 데이터셋 | uspto-grants-2001_12 |
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| ORD ID | ord-7988fd239167492c82cfcab229980e81 |
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| 출처 메모 | uspto-grants-2001_12 |
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