Benzyl chloroformate → 2-Benzyloxycarbonyloxyimino-2-phenylacetonitrile

HRID 1578218노트

반응식

HRID 1578218 반응식
Cl[C:2]([O:4][CH2:5][C:6]1[CH:11]=[CH:10][CH:9]=[CH:8][CH:7]=1)=[O:3].[OH:12][N:13]=[C:14]([C:17]1[CH:22]=[CH:21][CH:20]=[CH:19][CH:18]=1)[C:15]#[N:16].[OH-].[K+].O1CCOCC1>CCOCC>[CH2:5]([O:4][C:2]([O:12][N:13]=[C:14]([C:17]1[CH:22]=[CH:21][CH:20]=[CH:19][CH:18]=1)[C:15]#[N:16])=[O:3])[C:6]1[CH:11]=[CH:10][CH:9]=[CH:8][CH:7]=1

참가 물질

6

반응물 4

HCID 10387Benzyl chloroformateHCID 14797Potassium HydroxideHCID 312751,4-DioxaneHCID 699982-(Hydroxyimino)-2-phenylacetonitrile

생성물 1

HCID 540061222-Benzyloxycarbonyloxyimino-2-phenylacetonitrile수율 62.1%

시약·촉매·용매 1

HCID 3283Diethyl Ether용매

실험 절차

A solution of benzyl chloroformate (5.1 g.) in ether (40 ml.) was added to a solution of 2-hydroxyimino-2-phenylacetonitrile (4.4 g.) in a mixture of a 1 N potassium hydroxide aqueous solution (30 ml.) and dioxane (10 ml.) under ice-cooling. The mixture was stirred for 1 hour at the same temperature and for 4 hours at room temperature. The ether layer was separated from the reaction mixture and the aqueous layer was further extracted with ether. Both ether layers were combined, washed with water and dried over magnesium sulfate. The solvent was distilled off and n-hexane was added to the residue. The precipitated crystals were collected by filtration to give 2-benzyloxycarbonyloxyimino2-phenylacetonitrile (5.2 g.), mp 73° to 75° C.

후처리

  1. temperaturecooling
  2. customThe ether layer was separated from the reaction mixture
  3. extractionthe aqueous layer was further extracted with ether
  4. washwashed with water
  5. dry with materialdried over magnesium sulfate
  6. distillationThe solvent was distilled off
  7. additionn-hexane was added to the residue
  8. filtrationThe precipitated crystals were collected by filtration

출처 및 근거

ORD 기록
ord-a7855388df984f5d85178505e985881f
출처 데이터셋
uspto-grants-1981_09
특허 번호
USRE030752

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