Diisopropylethylamine → 4-Nitrophenyl 4,4,4-trifluorobutylcarbamate

HRID 589830

반응식

HRID 589830 반응식
[F:1][C:2]([F:8])([F:7])[CH2:3][CH2:4][CH2:5][NH2:6].Cl[C:10]([O:12][C:13]1[CH:18]=[CH:17][C:16]([N+:19]([O-:21])=[O:20])=[CH:15][CH:14]=1)=[O:11].C(N(C(C)C)CC)(C)C.C(=O)([O-])O.[Na+]>ClCCl>[F:1][C:2]([F:8])([F:7])[CH2:3][CH2:4][CH2:5][NH:6][C:10](=[O:11])[O:12][C:13]1[CH:14]=[CH:15][C:16]([N+:19]([O-:21])=[O:20])=[CH:17][CH:18]=1

참가 물질

6

반응 조건

온도
-15 °C

실험 절차

To a solution of 0.35 g (2.75 mmol) of 4,4,4-trifluoro-butylamine (CAS 819-46-5) in 20 ml of dichloromethane, cooled to −15° C., is added dropwise 1.00 g (4.96 mmol) of 4-nitrophenyl chloroformate (CAS 7693-46-1) dissolved in 15 ml of dichloromethane, while maintaining the temperature at −15° C. 0.48 ml (2.75 mmol) of diisopropylethylamine in 10 ml of dichloromethane still at −15° C. is then added. Stirring is continued at −15° C. for 45 minutes, and the temperature of the mixture is then allowed to return to 0° C. over 30 minutes. 20 ml of saturated aqueous sodium hydrogen carbonate solution are then added. The organic phase is separated out by settling and dried over sodium sulfate, and the solvent is partially evaporated off under reduced pressure to a volume of about 8 ml. This solution is chromatographed on a column of 40 g of silica gel, eluting with a mixture of 20% cyclohexane in dichloromethane, to give 0.76 g of 4-nitrophenyl 4,4,4-trifluorobutylcarbamate in the form of a white solid.

후처리

  1. waitto return to 0° C. over 30 minutes
  2. customThe organic phase is separated out
  3. dry with materialdried over sodium sulfate
  4. customthe solvent is partially evaporated off under reduced pressure to a volume of about 8 ml
  5. customThis solution is chromatographed on a column of 40 g of silica gel
  6. washeluting with a mixture of 20% cyclohexane in dichloromethane

출처 및 근거

ORD 기록
ord-bee3a2e119ef41469fffe701f59b535f
출처 데이터셋
uspto-grants-2016_01
특허 번호
US09233965B2

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