Hexane → (R)-1-bromo-1-[3,5-bis(trifluoromethyl)phenyl]ethane

HRID 1399513ノート

反応式

HRID 1399513 の反応式
Br[C:2](Cl)(Cl)[C:3]([Br:6])(Cl)Cl.C1(P(C2C=CC=CC=2)C2C=CC=CC=2)C=CC=CC=1.[F:28][C:29]([F:44])([F:43])[C:30]1[CH:31]=[C:32]([C@@H](O)C)[CH:33]=[C:34]([C:36]([F:39])([F:38])[F:37])[CH:35]=1.CCCCCC>C1(C)C=CC=CC=1>[Br:6][C@@H:3]([C:32]1[CH:33]=[C:34]([C:36]([F:39])([F:37])[F:38])[CH:35]=[C:30]([C:29]([F:28])([F:44])[F:43])[CH:31]=1)[CH3:2]

参加物

6

実験手順

Under an argon atmosphere, 1,2-dibromo-1,1,2,2-tetrachloroethane (7.57 g, 23.2 mmol) was dissolved in toluene (12.5 mL), the solution was added with triphenylphosphine (6.1 g, 23.2 mmol) at 0° C., and the mixture was stirred for 30 minutes. This reaction mixture was added dropwise with a solution of (S)-1-[3,5-bis(trifluoromethyl)phenyl]ethanol (1) (5.0 g, 19.4 mmol, >99.5% ee) in toluene (12.5 mL) at 0° C. over 10 minutes or more, and then the mixture was warmed to room temperature, and stirred for 1 hour at the same temperature. The reaction mixture was added with n-hexane (25 mL), and the mixture was filtered through Celite. The filtrate was successively washed with water, saturated aqueous sodium hydrogencarbonate, and saturated brine, dried over sodium sulfate, and then evaporated under reduced pressure. The resulting residue was distilled under reduced pressure (56° C., 0.7 mmHg) to obtain 5.52 g of (R)-1-bromo-1-[3,5-bis(trifluoromethyl)phenyl]ethane (2) as colorless oil (yield: 88.6%).

後処理

  1. stirringstirred for 1 hour at the same temperature
  2. filtrationthe mixture was filtered through Celite
  3. washThe filtrate was successively washed with water, saturated aqueous sodium hydrogencarbonate, and saturated brine
  4. dry with materialdried over sodium sulfate
  5. customevaporated under reduced pressure
  6. distillationThe resulting residue was distilled under reduced pressure (56° C., 0.7 mmHg)

出典と根拠

ORDレコード
ord-5b8f288919f142fe900d753a645c3f92
出典データセット
uspto-grants-2014_12
特許番号
US08906895B2

反応ノート

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