참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | 4-Toluenesulfonyl chloride | HCID 7397 | — |
| 반응물 | Diisopropylamine | HCID 7912 | — |
| 반응물 | 2-tert-Butylcyclohexanone | HCID 102681 | — |
| 용매 | Tetrahydrofuran | HCID 8028 | — |
| 생성물 | 2-Tert-butyl-6-chlorocyclohexanone | HCID 68680972 | 81% |
반응 단계
N-butyl lithium is added dropwise to a solution, cooled to 0° C., of diisopropylamine (5.5 mmol) in dry tetrahydrofuran. After the addition is complete the mixture is cooled to −78° C., and a solution of 2-tert-butylcyclohexanone (5 mmol) in dry tetrahydrofuran (50 ml) is introduced, followed by the addition of p-toluenesulphonyl chloride (5 mmol), also dissolved in dry tetrahydrofuran (50 ml). The reaction mixture is heated to room temperature and after stirring for 30 mins over silica gel filtered with ether as eluant. After concentration by evaporation in a vacuum 2-tert-butyl-6-chlorcyclohexanone (760 mg) is obtained in a yield of 81% (Tet. Lett. 1999, 40(12), 2231-2234).
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US07727979B2 |
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| 출처 데이터셋 | uspto-grants-2010_06 |
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| ORD ID | ord-2490bc6217a344258faf2fe00e97dd10 |
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| 출처 메모 | uspto-grants-2010_06 |
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