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HCID 22025443, 화합물 → HCID 17966419, 화합물

HRID 733263
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HRID 733263 반응식
[F:1][C:2]([F:20])([F:19])[CH2:3][N:4]1[C:12](=[O:13])[C:11]2[C:6](=[CH:7][CH:8]=[C:9]([C:14]([F:17])([F:16])[F:15])[CH:10]=2)[C:5]1=[O:18]>O>[OH:13][CH:12]1[C:11]2[C:6](=[CH:7][CH:8]=[C:9]([C:14]([F:16])([F:17])[F:15])[CH:10]=2)[C:5](=[O:18])[N:4]1[CH2:3][C:2]([F:19])([F:1])[F:20]
참가 물질반응 조건실험 절차후처리출처 및 근거반응 노트

참가 물질

3

반응물 1

HCID 22025443HCID 22025443, 화합물

생성물 1

HCID 17966419HCID 17966419, 화합물수율 75.8%

시약·촉매·용매 1

HCID 962Water용매

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온도
0 °C

실험 절차

5.5 g of 2-(2,2,2-trifluoro-ethyl)-5-trifluoromethyl-isoindole-1,3-dione were dissolved using 150 ml MeOH(anhydrous) and 1.0 g of KBH4 added at ambient temperature. The mixture was left at ambient temperature for 16 h, cooled to 0° C. and poured into 100 ml of water at 0° C. The methanol was removed in vacuo. The aqueous layer was extracted three times using 100 ml of CH2Cl2 each. The organic layer was dried over MgSO4 and the solvent was removed in vacuo to yield 4.2 g of a viscous oil (Rf(DIP)=0.37, MS (DCI): 300 (M+1)+).

후처리

  1. additionadded at ambient temperature
  2. customThe methanol was removed in vacuo
  3. extractionThe aqueous layer was extracted three times
  4. dry with materialThe organic layer was dried over MgSO4
  5. customthe solvent was removed in vacuo

출처 및 근거

ORD 기록
ord-d4549f63d0a54be49b1ae45fba4c5f08
출처 데이터셋
uspto-grants-2009_09
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07589117B2

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