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Ethanamine, 2,2,2-trifluoro- → HCID 22025443, 화합물

HRID 733264
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HRID 733264 반응식
[F:1][C:2]([F:15])([F:14])[C:3]1[CH:4]=[C:5]2[C:9](=[CH:10][CH:11]=1)[C:8](=[O:12])O[C:6]2=[O:13].[F:16][C:17]([F:21])([F:20])[CH2:18][NH2:19]>C1(C)C=CC(S(O)(=O)=O)=CC=1.CC(=O)OCC>[F:16][C:17]([F:21])([F:20])[CH2:18][N:19]1[C:6](=[O:13])[C:5]2[C:9](=[CH:10][CH:11]=[C:3]([C:2]([F:1])([F:15])[F:14])[CH:4]=2)[C:8]1=[O:12]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 2

HCID 9773Ethanamine, 2,2,2-trifluoro-HCID 127177895-(Trifluoromethyl)isobenzofuran-1,3-dione

생성물 1

HCID 22025443HCID 22025443, 화합물수율 80%

시약·촉매·용매 2

HCID 6101p-Toluenesulfonic acid촉매HCID 8857Ethyl Acetate용매

실험 절차

5.0 g of 5-trifluoromethyl-isobenzofuran-1,3-dione were dissolved using 50 ml of toluene(anhydrous) and 4.6 g of 2,2,2-trifluoro-ethylamine added. The mixture was left at ambient temperature for 16 h. 50 mg of toluene-4-sulfonic acid were then added and the mixture was refluxed for 5 h. 200 ml of EA were added and the mixture was washed twice using 50 ml of a 10% aqueous Na2CO3-solution. The organic layer was dried over MgSO4 and the solvent was removed in vacuo to yield 5.5 g of a viscous oil (Rf(DIP)=0.57; MS (EI): 298 (M+1)+).

후처리

  1. additionadded
  2. temperaturethe mixture was refluxed for 5 h
  3. washthe mixture was washed twice
  4. dry with materialThe organic layer was dried over MgSO4
  5. customthe solvent was removed in vacuo

출처 및 근거

ORD 기록
ord-08a39e5611d34ee1ac29f9391da919fa
출처 데이터셋
uspto-grants-2009_09
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07589117B2

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