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Dicyclohexylammonium (RS)-alpha-Methyl-3,5-bis(trifluoromethyl)benzeneacetate → 2-(3,5-Bis(trifluoromethyl)phenyl)propanoic acid

HRID 852676
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반응식

HRID 852676 반응식
[CH3:1][CH:2]([C:6]1[CH:11]=[C:10]([C:12]([F:15])([F:14])[F:13])[CH:9]=[C:8]([C:16]([F:19])([F:18])[F:17])[CH:7]=1)[C:3]([O-:5])=[O:4].C1([NH2+]C2CCCCC2)CCCCC1>C(OCC)(=O)C>[CH3:1][CH:2]([C:6]1[CH:7]=[C:8]([C:16]([F:17])([F:18])[F:19])[CH:9]=[C:10]([C:12]([F:13])([F:14])[F:15])[CH:11]=1)[C:3]([OH:5])=[O:4]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

3

반응물 1

HCID 86590571Dicyclohexylammonium (RS)-alpha-Methyl-3,5-bis(trifluoromethyl)benzeneacetate

생성물 1

HCID 115220582-(3,5-Bis(trifluoromethyl)phenyl)propanoic acid수율 100%

시약·촉매·용매 1

HCID 8857Ethyl Acetate용매

실험 절차

Dicyclohexylammonium (RS)-α-methyl-3,5-bis(trifluoromethyl)benzeneacetate (Description 4, 31.13 g, 67 mmol) was suspended in ethyl acetate and washed with aqueous citric acid (25%) and water, dried (MgSO4) and the solvent was evaporated under reduced pressure to give the title compound as a colourless solid (19.0 g, 100%). 1H NMR (400 MHz, CDCl3) δ 7.81 (1H, s), 7.78 (2H, s), 3.90 (1H, q, J 7.2 Hz), and 1.60 (3H, d, J 7.2 Hz).

후처리

  • washwashed with aqueous citric acid (25%) and water
  • dry with materialdried (MgSO4)
  • customthe solvent was evaporated under reduced pressure
  • 출처 및 근거

    ORD 기록
    ord-c90b80437c9b4bae9092e1d6cdf37e8d
    출처 데이터셋
    uspto-grants-2007_08
    DOI
    10.6084/m9.figshare.5104873.v1
    특허 번호
    US07253205B2

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