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4-Nitrophenyl chloroformate → 4-Nitrophenyl 2-trifluoroacetylaminoethyl carbonate

HRID 1156564
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HRID 1156564 반응식
[F:1][C:2]([F:10])([F:9])[C:3]([NH:5][CH2:6][CH2:7][OH:8])=[O:4].[N+:11]([C:14]1[CH:19]=[CH:18][C:17]([O:20][C:21](Cl)=[O:22])=[CH:16][CH:15]=1)([O-:13])=[O:12]>N1C=CC=CC=1>[C:21](=[O:22])([O:8][CH2:7][CH2:6][NH:5][C:3](=[O:4])[C:2]([F:10])([F:9])[F:1])[O:20][C:17]1[CH:16]=[CH:15][C:14]([N+:11]([O-:13])=[O:12])=[CH:19][CH:18]=1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 2

HCID 821294-Nitrophenyl chloroformateHCID 95211N-Trifluoroacetyl-2-aminoethanol

생성물 1

HCID 205350574-Nitrophenyl 2-trifluoroacetylaminoethyl carbonate

시약·촉매·용매 1

HCID 1049Pyridine용매

실험 절차

17 g (0.108 mol) of 2-(trifluoroacetylamino)ethanol are dissolved in 210 ml of pyridine, 21 g of chloroformic acid 4-nitrophenyl ester are added and the mixture is left to stand overnight at room temperature. It is then concentrated, the residue is taken up in methylene chloride and the methylene chloride mixture is washed with ice-water and dried with Na2SO4. After evaporating off the solvent, 33 g of a light-colored oil are obtained.

후처리

  1. waitthe mixture is left
  2. concentrationIt is then concentrated
  3. washthe methylene chloride mixture is washed with ice-water
  4. dry with materialdried with Na2SO4
  5. customAfter evaporating off the solvent, 33 g of a light-colored oil
  6. customare obtained

출처 및 근거

ORD 기록
ord-b11a788d0843406298d9b765a692d534
출처 데이터셋
uspto-grants-1982_06
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US04336369

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