関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|
| 反応物 | Dimethyl Sulfide | HCID 1068 | — |
| 反応物 | Hexane | HCID 8058 | — |
| 反応物 | N-bromobutanimide | HCID 67184 | — |
| 反応物 | (alphaR)-alpha-Methyl-3,5-bis(trifluoromethyl)benzenemethanol | HCID 2779031 | — |
| 溶媒 | Dichloromethane | HCID 6344 | — |
| 生成物 | (S)-1-(1-bromoethyl)-3,5-bis(trifluoromethyl)benzene | HCID 56654406 | 66% |
反応手順
Under an argon atmosphere, a suspension of N-bromosuccinimide (103 mg, 0.58 mmol) in anhydrous dichloromethane (2.0 mL) was added dropwise with dimethyl sulfide (53 μL, 0.70 mmol) under ice cooling over 3 minutes. The mixture was added dropwise with a solution of (R)-1-[3,5-bis(trifluoromethyl)phenyl]ethanol (100 mg, 0.39 mmol, >99.5% ee) in anhydrous dichloromethane (1 mL) at −20° C., and the mixture was stirred at room temperature for 6 hours. The reaction mixture was add with n-hexane, and the organic layer was washed with water and saturated brine, dried over anhydrous sodium sulfate, and then concentrated under reduced pressure. The resulting residue was purified by silica gel column chromatography (developing solvent, n-hexane) to obtain 82 mg of (S)-1-bromo-1-[3,5-bis(trifluoromethyl)phenyl]ethane as colorless oil.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 特許番号 | US09272966B2 |
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| 出典データセット | uspto-grants-2016_03 |
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| ORD ID | ord-95a292d379cf49a9a8287aa52a8348a5 |
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| 出典メモ | uspto-grants-2016_03 |
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