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Cornforth reagent → tert-Butyl methyl(4-oxobutyl)carbamate

HRID 2248622
ノート
印刷プレビュー

反応式

HRID 2248622 の反応式
[OH:1][CH2:2][CH2:3][CH2:4][CH2:5][N:6]([CH3:14])[C:7](=[O:13])[O:8][C:9]([CH3:12])([CH3:11])[CH3:10].[Cr](O[Cr]([O-])(=O)=O)([O-])(=O)=O.[NH+]1C=CC=CC=1.[NH+]1C=CC=CC=1>ClCCl>[CH3:14][N:6]([CH2:5][CH2:4][CH2:3][CH:2]=[O:1])[C:7](=[O:13])[O:8][C:9]([CH3:12])([CH3:10])[CH3:11]
参加物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 2724130Cornforth reagentHCID 14854943tert-Butyl (4-hydroxybutyl)(methyl)carbamate

生成物 1

HCID 15078448tert-Butyl methyl(4-oxobutyl)carbamate収率 70%

試薬・触媒・溶媒 1

HCID 6344Dichloromethane溶媒2 回

実験手順

A solution of 50 parts of (1,1-dimethylethyl) (4-hydroxybutyl)methylcarbamate in 91 parts of dichloromethane was added dropwise to a mixture of 150 parts of pyridinium dichromate, 112 parts of molecular sieves and 1300 parts of dichloromethane at a temperature about 10° C. Upon completion, stirring was continued for 3 hours at room temperature. The reaction mixture was filtered, washed with 1,1'-oxybisethane and the filtrate was evaporated. The residue was purified by column chromatography over silica gel using dichloromethane as eluent. The pure fractions were collected and the eluent was evaporated with methylbenzene, yielding 35 parts (70%) of (1,1-dimethylethyl) methyl(4-oxobutyl)carbamate as a residue (int. 38).

後処理

  1. filtrationThe reaction mixture was filtered
  2. washwashed with 1,1'-oxybisethane
  3. customthe filtrate was evaporated
  4. customThe residue was purified by column chromatography over silica gel
  5. customThe pure fractions were collected
  6. customthe eluent was evaporated with methylbenzene

出典と根拠

ORDレコード
ord-6333324afbd543bc85d35f00cbeab497
出典データセット
uspto-grants-1991_08
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US05041454

反応ノート

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