Potassium Fluoride → ((S)-2-Fluoro-1-methyl-ethyl)-benzene

HRID 390296

反応式

HRID 390296 の反応式
[C:1]1([C@H:7]([CH3:20])[CH2:8]OS(C2C=CC(C)=CC=2)(=O)=O)[CH:6]=[CH:5][CH:4]=[CH:3][CH:2]=1.[F-:21].[K+]>[Cl-].[Na+]>[F:21][CH2:8][C@H:7]([C:1]1[CH:6]=[CH:5][CH:4]=[CH:3][CH:2]=1)[CH3:20]

参加物

4

反応条件

温度
62.5 °C

実験手順

9.62 g of toluene-4-sulfonic acid (S)-2-phenyl-propyl ester (33.13 mmol) were dissolved in 80 ml of polyethylenglycol 400. 9.62 g of potassium fluoride (165.6 mmol) were added and the reaction mixture was stirred at 50° C. for 3 days and another 2 days at 55-70° C. The reaction was treated with 150 ml of saturated aqueous sodium chloride solution, extracted three times with diethyl ether, and the combined organic layers were dried over magnesium sulfate, filtered, and the solvent was evaporated under reduced pressure. The crude product was purified via silica gel chromatography using cyclohexyane/ethyl acetate 15% as eluent. 2.85 g of the desired product were isolated, containing ˜25% of the elimination side product.

後処理

  1. extractionextracted three times with diethyl ether
  2. dry with materialthe combined organic layers were dried over magnesium sulfate
  3. filtrationfiltered
  4. customthe solvent was evaporated under reduced pressure
  5. customThe crude product was purified via silica gel chromatography

出典と根拠

ORDレコード
ord-ef6b8afa825a467996e6eaf7f26a9c17
出典データセット
uspto-grants-2013_02
特許番号
US08383641B2

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