참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Triethylamine | HCID 8471 | — |
| 반응물 | Sodium Hydroxide | HCID 14798 | — |
| 반응물 | Trifluoromethanesulfonic acid | HCID 62406 | — |
| 반응물 | Bisulfite | HCID 104748 | — |
| 반응물 | 2,3,4-Trifluorophenol | HCID 123174 | — |
| 반응물 | N,N-Diethylethanamine trihydrofluoride | HCID 175505 | — |
| 반응물 | 2-(6-{4-n-Propylcyclohexyl}spiro[3.3]hept-2-ylidene)[1,3]dithiane | HCID 58596254 | — |
| 용매 | Dichloromethane | HCID 6344 | — |
| 생성물 | HCID 58596253 | HCID 58596253 | — |
반응 단계
10.0 g (29.7 mmol) of the dithioacetal 6 are dissolved in 100 ml of dichloro-methane, and 2.6 ml (30.0 mmol) of trifluoromethanesulfonic acid are added dropwise with ice/common salt cooling. After 5 minutes, the cooling is removed, and the batch is stirred at room temperature for 45 minutes. The batch is subsequently cooled to −70° C., a mixture of 7.5 ml (54.0 mmol) of triethylamine and 6.67 g (45.0 mmol) of trifluorophenol in 30 ml of dichloromethane is added, and the mixture is stirred at −70° C. for 1 hour. 24.2 ml (0.150 mol) of triethylamine tris(hydrofluoride) are then added, and, after 5 minutes, 42.9 g (0.150 mol) of DBH, suspended in 60 ml of dichloromethane, are added in portions over the course of about 30 minutes. After 90 minutes, the batch is allowed to thaw and is hydro-lysed using 1 M sodium hydroxide solution and aqueous hydrogen sulfite solution. The organic phase is separated off, washed with saturated sodium chloride solution and dried over sodium sulfate. The solvent is removed under reduced pressure, and the residue is filtered through silica gel with n-heptane, giving the spiro compound 7 as a colourless solid of melting point: 43° C.
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US07270856B2 |
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| 출처 데이터셋 | uspto-grants-2007_09 |
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| ORD ID | ord-25a79e9603f9477286e0a964f64d4e1e |
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| 출처 메모 | uspto-grants-2007_09 |
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