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Water → Phenyl hydrogen benzylcarbonimidate

HRID 426766
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HRID 426766 반응식
[CH2:1]([NH2:8])[C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=1.Cl[C:10]([O:12][C:13]1[CH:18]=[CH:17][CH:16]=[CH:15][CH:14]=1)=[O:11].C(=O)([O-])[O-].[K+].[K+].O>O1CCOCC1>[CH2:1]([NH:8][C:10](=[O:11])[O:12][C:13]1[CH:18]=[CH:17][CH:16]=[CH:15][CH:14]=1)[C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

6

반응물 4

HCID 962WaterHCID 7504BenzylamineHCID 11430Potassium CarbonateHCID 15891Phenyl chloroformate

생성물 1

HCID 176410Phenyl hydrogen benzylcarbonimidate

시약·촉매·용매 1

HCID 312751,4-Dioxane용매

실험 절차

Benzylamine (53.5 g.) is added during 30 minutes to a stirred suspension of phenyl chloroformate (78.3 g.) and anhydrous potassium carbonate (151.8 g.) in dioxan (500 ml.) and the mixture is stirred at laboratory temperature for 72 hours and then poured into water. The mixture is extracted with ethyl acetate and the extract is washed with water, dried over magnesium sulphate and evaporated to dryness. The residue is stirred with petroleum ether (b.p. 60°-80° C.) and the mixture is filtered. There is thus obtained as solid residue phenyl N-benzylcarbamate, which is used without further purification.

후처리

  1. extractionThe mixture is extracted with ethyl acetate
  2. washthe extract is washed with water
  3. dry with materialdried over magnesium sulphate
  4. customevaporated to dryness
  5. stirringThe residue is stirred with petroleum ether (b.p. 60°-80° C.)
  6. filtrationthe mixture is filtered

출처 및 근거

ORD 기록
ord-4d6b2bd4e945483598674c8ec0696d8f
출처 데이터셋
uspto-grants-1979_10
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US04171374

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