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2-Propenoic acid, 3-[4-(trifluoromethyl)phenyl]-, ethyl ester → (E)-3-(4-(trifluoromethyl)phenyl)prop-2-en-1-ol

HRID 1601366
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HRID 1601366 반응식
[F:1][C:2]([F:17])([F:16])[C:3]1[CH:15]=[CH:14][C:6](/[CH:7]=[CH:8]/[C:9](OCC)=[O:10])=[CH:5][CH:4]=1.[H-].C([Al+]CC(C)C)C(C)C.C1(C)C=CC=CC=1>C1(C)C=CC=CC=1>[F:1][C:2]([F:16])([F:17])[C:3]1[CH:15]=[CH:14][C:6](/[CH:7]=[CH:8]/[CH2:9][OH:10])=[CH:5][CH:4]=1
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참가 물질

4

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HCID 115070152-Propenoic acid, 3-[4-(trifluoromethyl)phenyl]-, ethyl esterHCID 86583787Diisobutylaluminumhydride toluene

생성물 1

HCID 10512285(E)-3-(4-(trifluoromethyl)phenyl)prop-2-en-1-ol수율 96%

시약·촉매·용매 1

HCID 1140Toluene용매

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온도
0 °C

실험 절차

In 15 ml of toluene were dissolved 3.00 g (12.3 mmol) of ethyl trans-4-(trifluoromethyl)cinnamate, and 16.4 ml (24.6 mmol) of a 1.5M diisobutyl aluminum hydride-toluene solution were added to the solution with stirring at 0° C. After 20 minutes, ice-water was added to the reaction mixture and the mixture was stirred for 10 minutes, followed by removal of the insolubles by filtration using Celite. The filtrate was extracted with ethyl acetate and, after drying, the solvent was distilled off to obtain a crystalline residue. The residue was recrystallized from a mixed solvent of benzene-hexane to obtain 2.36 g (yield: 96%) of the title compound having a melting point of 53 to 55° C.

후처리

  1. additionwere added to the solution
  2. stirringthe mixture was stirred for 10 minutes
  3. customfollowed by removal of the insolubles by filtration
  4. extractionThe filtrate was extracted with ethyl acetate
  5. customafter drying
  6. distillationthe solvent was distilled off
  7. customto obtain a crystalline residue
  8. customThe residue was recrystallized from a mixed solvent of benzene-hexane

출처 및 근거

ORD 기록
ord-4a627d93cc344a16afab0ee5fa969d3b
출처 데이터셋
uspto-grants-1999_11
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US05977152

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