참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Water | HCID 962 | — |
| 반응물 | 1,2,3,4-Tetrahydrocarbazole | HCID 13664 | — |
| 반응물 | Sodium Hydroxide | HCID 14798 | — |
| 반응물 | Borane;tetrahydrofuran | HCID 2723981 | — |
| 용매 | Trifluoroacetic acid | HCID 6422 | — |
| 용매 | Tetrahydrofuran | HCID 8028 | — |
| 생성물 | 2,3,4,4a,9,9a-Hexahydro-1H-carbazole | HCID 101162 | 80% |
반응 단계
1,2,3,4-Tetrahydrocarbazole (75 milligrams) was dissolved under nitrogen in 3 milliliters of trifluoroacetic acid. To the mixture, cooled in a water bath, was added dropwise about 1.5 milliliters of an about 1 M BH3.THF in tetrahydrofuran. The mixture was stirred at room temperature for about 45 minutes. Thereafter, water (1 milliliter) was added slowly and the resulting solution stirred for 10 minutes. The solution was then made basic with 10 percent aqueous sodium hydroxide, and the basic solution extracted with methylene chloride. The organic methylene chloride layer was washed once with saturated sodium chloride, dried over potassium carbonate, and evaporated in vacuo to obtain 60 milligrams (80 percent yield) of a crystalline 1,2,3,4,4a,9a-hexahydrocarbazole product, m.p., 93°-96° C.
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US04210590 |
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| 출처 데이터셋 | uspto-grants-1980_07 |
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| ORD ID | ord-04c9230717ec428d9d3763e4efae0d9a |
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| 출처 메모 | uspto-grants-1980_07 |
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