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

HRID 870335
ノート
印刷プレビュー

反応式

HRID 870335 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]
参加物反応条件実験手順後処理出典と根拠反応ノート

参加物

4

反応物 2

HCID 522689Potassium FluorideHCID 13791931Toluene-4-sulfonic acid (S)-2-phenyl-propyl ester

生成物 1

HCID 53628601((S)-2-Fluoro-1-methyl-ethyl)-benzene収率 62.3%

試薬・触媒・溶媒 1

HCID 5234Sodium Chloride溶媒

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 polyethyleneglycol 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 cyclohexane/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-aca7b4f44b014699b7dab0bcaa9a01df
出典データセット
uspto-grants-2015_03
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US08969552B2

反応ノート

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このページの内容参加物反応条件実験手順後処理出典と根拠反応ノート