Diethyl Ether → HCID 13560729、化合物

HRID 414837ノート

反応式

HRID 414837 の反応式
[OH:1][C:2]1[CH:3]=[C:4]([CH:8]([OH:14])[CH2:9][CH2:10][CH2:11][CH2:12][CH3:13])[CH:5]=[CH:6][CH:7]=1.[Cr](Cl)([O-])(=O)=O.[NH+:20]1[CH:25]=[CH:24][CH:23]=[CH:22][CH:21]=1.[C:26]([O-])(=O)[CH3:27].[Na+].[CH3:31][CH2:32]OCC.[CH2:36](Cl)Cl>>[C:8]([C:4]1[CH:3]=[C:2]([CH:7]=[CH:6][CH:5]=1)[O:1][CH2:36][C:21]1[CH:22]=[CH:23][C:24]2[C:25](=[CH:31][CH:32]=[CH:26][CH:27]=2)[N:20]=1)(=[O:14])[CH2:9][CH2:10][CH2:11][CH2:12][CH3:13].[C:8]([C:4]1[CH:3]=[C:2]([OH:1])[CH:7]=[CH:6][CH:5]=1)(=[O:14])[CH2:9][CH2:10][CH2:11][CH2:12][CH3:13]

参加物

7

実験手順

A solution of 1-(3-hydroxyphenyl)-1-hexanol (3 g) in methylene chloride (200 ml) was added to a well-stirred suspension of pyridinium chlorochromate (5.1 g) and sodium acetate (2.5 g) in methylenechloride (150 ml). The mixture was stirred at room temperature for two hours. Ether (100 ml) was added, and the brown granular preiipitate was removed by filtration. All volatiles were removed from the filtrate, and the residual liquid was purified by chromtography on silica gel using ether as eluent. The desired ketone, 3-hexanoylphenol, was isolated as a clear, colorless oil.

後処理

  1. customthe brown granular preiipitate was removed by filtration
  2. customAll volatiles were removed from the filtrate
  3. customthe residual liquid was purified by chromtography on silica gel

出典と根拠

ORDレコード
ord-58b90a92d20b4fa4ac3e845e68d8004b
出典データセット
uspto-grants-1988_12
特許番号
US04794188

反応ノート

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