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Oxygen → Benzenepropanoic acid, α-methyl-4-(trifluoromethyl)-, ethyl ester

HRID 1500234
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반응식

HRID 1500234 반응식
[CH3:1]/[C:2](=[CH:8]\[C:9]1[CH:14]=[CH:13][C:12]([C:15]([F:18])([F:17])[F:16])=[CH:11][CH:10]=1)/[C:3]([O:5][CH2:6][CH3:7])=[O:4].O=O>[Pd].CO>[CH3:1][CH:2]([CH2:8][C:9]1[CH:10]=[CH:11][C:12]([C:15]([F:16])([F:18])[F:17])=[CH:13][CH:14]=1)[C:3]([O:5][CH2:6][CH3:7])=[O:4]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 2

HCID 977OxygenHCID 102180854HCID 102180854, 화합물

생성물 1

HCID 90111382Benzenepropanoic acid, α-methyl-4-(trifluoromethyl)-, ethyl ester수율 91.8%

시약·촉매·용매 2

HCID 23938Palladium촉매2회HCID 887Methanol용매

실험 절차

Dissolve ethyl(E)-2-methyl-3-[4-(trifluoromethyl)phenyl]prop-2-enoate (2.58 g, 10 mmol) in a suspension of 10 wt % Pd—C (258 mg)/MeOH (20 mL) in an RBF under nitrogen, as exposure of Pd—C to oxygen can lead to fire. Carefully purge the flask with hydrogen and stir the resulting mixture under hydrogen (1 Atm) for 16 h. Purge the flask nitrogen and degas the solvent to remove all hydrogen before exposing to air. Filter the suspension through a pad of celite. Concentrate the filtrate to give the title compound (2.39 g).

후처리

  1. customCarefully purge the flask with hydrogen
  2. customPurge the flask nitrogen
  3. customdegas the solvent
  4. customto remove all hydrogen
  5. filtrationFilter the suspension through a pad of celite
  6. concentrationConcentrate the filtrate

출처 및 근거

ORD 기록
ord-c2290072995c492a97beb5903e224760
출처 데이터셋
uspto-grants-2015_12
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US09206139B2

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