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Cornforth reagent → Methyl(4-oxobutyl)carbamate

HRID 654172
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HRID 654172 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](C)[C:28](=[O:34])[O:29][C:30](C)(C)C>ClCCl>[CH3:30][O:29][C:28](=[O:34])[NH:27][CH2:26][CH2:25][CH2:24][CH:23]=[O:22]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 2

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

생성물 1

HCID 19888448Methyl(4-oxobutyl)carbamate

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'-oxydisethane and the filtreate 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'-oxydisethane
  5. customthe filtreate 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-4d2f3908518a4ddab1cf8f375773f0ed
출처 데이터셋
uspto-grants-1992_07
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US05130312

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