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

HRID 1165035
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HRID 1165035 반응식
[Cr](O[Cr]([O-])(=O)=O)([O-])(=O)=O.[NH+]1C=CC=CC=1.[NH+]1C=CC=CC=1.[OH:22][CH2:23][CH2:24][CH2:25][CH2:26][N:27]([CH3:35])[C:28](=[O:34])[O:29][C:30]([CH3:33])([CH3:32])[CH3:31]>ClCCl>[CH3:35][N:27]([CH2:26][CH2:25][CH2:24][CH:23]=[O:22])[C:28](=[O:34])[O:29][C:30]([CH3:33])([CH3:31])[CH3:32]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 2

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

생성물 1

HCID 15078448tert-Butyl methyl(4-oxobutyl)carbamate수율 6.9%

시약·촉매·용매 1

HCID 6344Dichloromethane용매2회

실험 절차

To a stirred and cooled (<10° C.) solution of 150 parts of pyridinium dichromate in 1300 parts of dichloromethane was added dropwise a solution of 50 parts of (1,1-dimethylethyl) (4-hydroxybutyl)methylcarbamate in 91 parts of dichloromethane. Upon complete addition, stirring was continued for 3 hours in the presence of 112 parts of molecular sieves of 4A at room temperature. The reaction mixture was filtered over magnesium sulfate, 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. The residue was taken up in methylbenzene and the whole was evaporated again, yielding 3.5 parts (6.9%) of (1,1-dimethylethyl) methyl(4-oxobutyl)carbamate as a residue (interm. 7).

후처리

  1. additionUpon complete addition
  2. stirringstirring
  3. filtrationThe reaction mixture was filtered over magnesium sulfate
  4. washwashed with 1,1'-oxybisethane
  5. customthe filtrate was evaporated
  6. customThe residue was purified by column chromatography over silica gel
  7. customThe pure fractions were collected
  8. customthe eluent was evaporated
  9. customthe whole was evaporated again

출처 및 근거

ORD 기록
ord-0014caa4e6104baab04266c7a31755d2
출처 데이터셋
uspto-grants-1990_03
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US04906643

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