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Water → 3,3,3-Trifluoro-2-phenylpropanoic acid

HRID 2393915
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HRID 2393915 반응식
[F:1][C:2]([F:18])([F:17])[C:3]([C:11]1[CH:16]=[CH:15][CH:14]=[CH:13][CH:12]=1)(C(F)(F)F)[C:4]([OH:6])=[O:5].[OH-].[Na+].O>CO>[F:1][C:2]([F:17])([F:18])[CH:3]([C:11]1[CH:12]=[CH:13][CH:14]=[CH:15][CH:16]=1)[C:4]([OH:6])=[O:5]
참가 물질반응 조건실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 3

HCID 962WaterHCID 14798Sodium HydroxideHCID 11821736HCID 11821736, 화합물

생성물 1

HCID 2872493,3,3-Trifluoro-2-phenylpropanoic acid수율 62%

시약·촉매·용매 1

HCID 887Methanol용매

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온도
90 °C

실험 절차

2.9 g (10 millimole) of methyl ester of α,α-bis(trifluoromethyl)phenylacetic acid, 2.5 g (63 millimole) of sodium hydroxide, 3.0 g of water and 3.0 ml of methanol were charged into an eggplant-type flask having a capacity of 100 ml, provided with a marine-type condenser and refluxed at a bath temperature of 90° C. for 6 hours. Methanol was distilled off from the reaction mixture under reduced pressure, and the residue was dissolved in 30 ml of 3N hydrochloric acid and then extracted with ether. The ether layer was dried with anhydrous MgSO4 and then concentrated under reduced pressure. The thus obtained residue was subjected to silica gel column chromatography, using n-hexane/dichloromethane as a mobile phase, whereby 1.26 g of α-(trifluoromethyl)phenylacetic acid was obtained (yield: 62%).

후처리

  1. customprovided with a marine-type condenser
  2. distillationMethanol was distilled off from the reaction mixture under reduced pressure
  3. dissolutionthe residue was dissolved in 30 ml of 3N hydrochloric acid
  4. extractionextracted with ether
  5. dry with materialThe ether layer was dried with anhydrous MgSO4
  6. concentrationconcentrated under reduced pressure

출처 및 근거

ORD 기록
ord-5b03f446834c4d9e85c13d6a3ccc98d8
출처 데이터셋
uspto-grants-1998_09
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US05808132

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