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

HRID 2248622
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HRID 2248622 반응식
[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]
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참가 물질

4

반응물 2

HCID 2724130Cornforth reagentHCID 14854943tert-Butyl (4-hydroxybutyl)(methyl)carbamate

생성물 1

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

시약·촉매·용매 1

HCID 6344Dichloromethane용매2회

실험 절차

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).

후처리

  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

출처 및 근거

ORD 기록
ord-6333324afbd543bc85d35f00cbeab497
출처 데이터셋
uspto-grants-1991_08
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US05041454

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