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Imidazole → (S)-3-(tert-butyldimethylsilyloxy)-1-(4-chloro-3-fluorophenyl)propan-1-ol

HRID 2365806
ノート
印刷プレビュー

反応式

HRID 2365806 の反応式
[Cl:1][C:2]1[CH:7]=[CH:6][C:5]([C@@H:8]([OH:12])[CH2:9][CH2:10][OH:11])=[CH:4][C:3]=1[F:13].N1C=CN=C1.[Si:19](Cl)([C:22]([CH3:25])([CH3:24])[CH3:23])([CH3:21])[CH3:20]>ClCCl>[Si:19]([O:11][CH2:10][CH2:9][C@@H:8]([C:5]1[CH:6]=[CH:7][C:2]([Cl:1])=[C:3]([F:13])[CH:4]=1)[OH:12])([C:22]([CH3:25])([CH3:24])[CH3:23])([CH3:21])[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

5

反応物 3

HCID 795ImidazoleHCID 28928tert-Butyldimethylsilyl chlorideHCID 86696659(S)-1-(4-chloro-3-fluorophenyl)propane-1,3-diol

生成物 1

HCID 86696660(S)-3-(tert-butyldimethylsilyloxy)-1-(4-chloro-3-fluorophenyl)propan-1-ol収率 51.3%

試薬・触媒・溶媒 1

HCID 6344Dichloromethane溶媒2 回

反応条件

温度
0 °C

実験手順

(S)-1-(4-Chloro-3-fluorophenyl)propane-1,3-diol (10.5 g, 51.3 mmol) was dissolved in dichloromethane (200 mL), and imidazole (8.73 g, 128 mmol) was added. The mixture was then cooled to 0° C., and tert-butyldimethylsilyl chloride (9.67 g, 64.1 mmol) was added. The mixture was agitated for 1 hour, diluted with dichloromethane to 250 mL and washed with water, sodium bicarbonate solution, dried and evaporated. Purified by chromatography on silica gel, eluted with 5-10% ethyl acetate/hexanes to give (S)-3-(tert-butyldimethylsilyloxy)-1-(4-chloro-3-fluorophenyl)propan-1-ol (8.40 g, 26.3 mmol, 51.3% yield) as an oil.

後処理

  1. washwashed with water, sodium bicarbonate solution
  2. customdried
  3. customevaporated
  4. customPurified by chromatography on silica gel
  5. washeluted with 5-10% ethyl acetate/hexanes

出典と根拠

ORDレコード
ord-6f3b4cab0e6c490cbcd76f3f05490525
出典データセット
uspto-grants-2014_04
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US08697715B2

反応ノート

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