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Ethanamine, 2,2,2-trifluoro- → HCID 14801043, 화합물

HRID 1493205
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HRID 1493205 반응식
[C:1]([C:5]1[CH:15]=[CH:14][C:8]([C:9]([N:11]=[C:12]=[S:13])=O)=[CH:7][CH:6]=1)([CH3:4])([CH3:3])[CH3:2].[F:16][C:17]([F:21])([F:20])[CH2:18][NH2:19]>>[C:1]([C:5]1[CH:15]=[CH:14][C:8]([CH2:9][NH:11][C:12]([NH:19][CH2:18][C:17]([F:21])([F:20])[F:16])=[S:13])=[CH:7][CH:6]=1)([CH3:4])([CH3:3])[CH3:2]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

3

반응물 2

HCID 9773Ethanamine, 2,2,2-trifluoro-HCID 27953844-Tert-butylbenzoyl isothiocyanate

생성물 1

HCID 14801043HCID 14801043, 화합물수율 105.2%

실험 절차

10.82 g of 4-t-butylbenzoyl isothiocyanate obtawined in (1) and 7.54 g of 2,2,2-trifluoroethylamine were dissolved in 20 ml of ethyl acetawte. The solution was left to stand at room temperature for 24 houirs. Ethyl acetate was evaporated under reduced prerssure. The resultilng oily product was purified by column chromatography silica gel; developing solvent hexane/ethyl acetate (4:1)) to give 15.80 g of the desired 1-(4-t-butylbenzyl)-3-(2,2,2-trifluoroethyl)thiourea.

후처리

  1. dissolutionwere dissolved in 20 ml of ethyl acetawte
  2. waitThe solution was left
  3. customto stand at room temperature for 24 houirs
  4. customEthyl acetate was evaporated under reduced prerssure
  • customThe resultilng oily product was purified by column chromatography silica gel
  • 출처 및 근거

    ORD 기록
    ord-33224c63a543431fa998cd259b2bfb6c
    출처 데이터셋
    uspto-grants-1991_06
    DOI
    10.6084/m9.figshare.5104873.v1
    특허 번호
    US05021412

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