참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Hydrochloric Acid | HCID 313 | — |
| 반응물 | Water | HCID 962 | — |
| 반응물 | Acetonitrile | HCID 6342 | — |
| 반응물 | Indoline | HCID 10328 | — |
| 반응물 | Boron tribromide | HCID 25134 | — |
| 반응물 | Aluminum(III) Chloride | HCID 6451240 | — |
| 용매 | Toluene | HCID 1140 | — |
| 생성물 | 1-(2,3-Dihydro-1H-indol-7-yl)ethan-1-one | HCID 13699421 | — |
반응 단계
To a solution of 47.35 g. (0.5 mole) of boron tribromide in 300 ml. of toluene at 0° C. was added dropwise a solution of 50 g. (0.42 mole) of indoline and 22.39 g. (0.546 mole) of acetonitrile in 200 ml. of toluene. After stirring for 10 minutes 67.2 g. (0.5 mole) of aluminum chloride was added in portions. The resulting reaction mixture was heated to reflux for 66 hours, cooled to 5° C. and treated with 80 ml. of water and 330 ml. of 2N hydrochloric acid. The resulting mixture was heated to reflux for 2.5 hours, cooled and filtered. The filtrate was set aside and the solids suspended in 500 ml. of water and treated with 2N sodium hydroxide solution until basic. The basic mixture was extracted (2×200 ml.) with methylene chloride and the organic phase separated, dried and concentrated to a solid, 17.2 g. The filtrate which was set aside was made basic with 4N aqueous sodium hydroxide and extracted with methylene chloride. The organic phase was separated, dried and concentrated to a solid, 21.8 g. The combined solids were recrystallized from hexane, 30 g., m.p. 83°-85° C.
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US04725616 |
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| 출처 데이터셋 | uspto-grants-1988_02 |
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| ORD ID | ord-5795629fb40746d085bc44f1d0c40b6a |
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| 출처 메모 | uspto-grants-1988_02 |
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