Ethyl trimethylsilylacetate → Ethyl 3-(4-fluorophenyl)-3-(4-hydroxyphenyl)-acrylate

HRID 731168

反応式

HRID 731168 の反応式
C[Si](C)(C)[N-][Si](C)(C)C.[Li+].C[Si]([CH2:15][C:16]([O:18][CH2:19][CH3:20])=[O:17])(C)C.[F:21][C:22]1[CH:27]=[CH:26][C:25]([C:28]([C:30]2[CH:35]=[CH:34][C:33]([OH:36])=[CH:32][CH:31]=2)=O)=[CH:24][CH:23]=1>C1COCC1>[F:21][C:22]1[CH:23]=[CH:24][C:25]([C:28]([C:30]2[CH:35]=[CH:34][C:33]([OH:36])=[CH:32][CH:31]=2)=[CH:15][C:16]([O:18][CH2:19][CH3:20])=[O:17])=[CH:26][CH:27]=1

参加物

5

実験手順

A solution of lithium hexamethyldisilazide (23.1 mL, 1 M in THF) was added to a stirred solution of ethyl (trimethylsilyl)acetate (2.53 mL, 13.9 mmol) in THF (15 mL) in 10 minutes at −78° C. The reaction mixture was further stirred at this temperature for 20 minutes. A solution of (4-fluoro-phenyl)-(4-hydroxy-phenyl)-methanone (2 g, 9.2 mmol) in THF (30 mL) was slowly added to the reaction mixture. The reaction mixture was brought to 0° C. over 5 hours. The reaction mixture was quenched with saturated ammonium chloride solution, extracted into EtOAc and washed with dilute ammonium chloride solution. The organic layer was dried over magnesium sulfate. The solvent was removed under vacuum, and the resulting product was flash chromatographed on silica gel, giving M1.1 as an oil.

後処理

  1. waitThe reaction mixture was brought to 0° C. over 5 hours
  2. customThe reaction mixture was quenched with saturated ammonium chloride solution
  3. extractionextracted into EtOAc
  4. washwashed with dilute ammonium chloride solution
  5. dry with materialThe organic layer was dried over magnesium sulfate
  6. customThe solvent was removed under vacuum
  7. customchromatographed on silica gel
  8. customgiving M1.1 as an oil

出典と根拠

ORDレコード
ord-c3b17590bdc5410d85a69b887de178d7
出典データセット
uspto-grants-2009_09
特許番号
US07582803B2

関連ノート

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