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HRID 918949作成日:2026年10月27日

Dimethyl Sulfide → (S)-1-(1-bromoethyl)-3,5-bis(trifluoromethyl)benzene

https://huagongshe.com/reaction/918949

反応式

関与物質

役割名称HCID仕込み量
反応物Dimethyl SulfideHCID 1068—
反応物HexaneHCID 8058—
反応物N-bromobutanimideHCID 67184—
反応物(alphaR)-alpha-Methyl-3,5-bis(trifluoromethyl)benzenemethanolHCID 2779031—
溶媒DichloromethaneHCID 6344—
生成物(S)-1-(1-bromoethyl)-3,5-bis(trifluoromethyl)benzeneHCID 5665440666%

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

DOI10.6084/m9.figshare.5104873.v1
特許番号US09272966B2
出典データセットuspto-grants-2016_03
ORD IDord-95a292d379cf49a9a8287aa52a8348a5
出典メモuspto-grants-2016_03