Sodium Hydroxide → 2-Cyclopropyl-4-(trifluoromethyl)benzoic acid

HRID 1690274

Reaktionsgleichung

C[O:2][C:3](=[O:17])[C:4]1[CH:9]=[CH:8][C:7]([C:10]([F:13])([F:12])[F:11])=[CH:6][C:5]=1[CH:14]1[CH2:16][CH2:15]1.[OH-].[Na+]>C(O)C>[CH:14]1([C:5]2[CH:6]=[C:7]([C:10]([F:11])([F:12])[F:13])[CH:8]=[CH:9][C:4]=2[C:3]([OH:17])=[O:2])[CH2:16][CH2:15]1

Komponenten

Reaktionsbedingungen

Temperatur: 80 °C

Versuchsvorschrift

To a suspension of 485 mg (1.986 mmol) 2-cyclopropyl-4-trifluoromethyl-benzoic acid methyl ester in 8 ml ethanol at room temperature, was added 1.99 ml (3.972 mmol) 2N NaOH. The mixture was heated in an 80° C. oil bath for 30 minutes. The solution was cooled to room temperature and the ethanol was evaporated. The residue was diluted with water, acidified with 2N HCl to pH 2 and dichloromethane was added. The aqueous phase was extracted twice with dichloromethane. The combined organic phases were dried over sodium sulfate, filtered and concentrated in vacuo. The crude product was purified on silica gel (Eluent: Heptane/ethyl acetate 0 to 100%) to provide 0.197 g (27%) of the title compound as a light yellow solid. MS (m/e): 229.0 (M−H)

Aufarbeitung

temperatureThe solution was cooled to room temperature
customthe ethanol was evaporated
additionThe residue was diluted with water
additionwas added
extractionThe aqueous phase was extracted twice with dichloromethane
dry with materialThe combined organic phases were dried over sodium sulfate
filtrationfiltered
concentrationconcentrated in vacuo
customThe crude product was purified on silica gel (Eluent: Heptane/ethyl acetate 0 to 100%)

Quellen und Nachweise

ORD-Eintrag: ord-c2d8fa6ab09f4345879d6893e057278a
Quelldatensatz: uspto-grants-2012_04
DOI: 10.6084/m9.figshare.5104873.v1
Patentnummer: US08153653B2

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