Hydrochloric Acid → 4-(1,1-Difluoroethyl)benzaldehyde

To a solution of 1-bromo-4-(1,1-difluoroethyl)benzene (1.00 g) in tetrahydrofuran (10.0 mL), n-butyl lithium (2.69 mol/L, solution in n-hexane, 1.68 mL) was added at −80° C. and the mixture was stirred at that temperature for 5 minutes. Subsequently, N,N-dimethylformamide (0.522 mL) was added at −80° C. and after stirring the mixture at that temperature for 20 minutes, 2 mol/L hydrochloric acid (2.50 mL) was added. After bringing the reaction mixture to room temperature, two extractions were conducted with ethyl acetate and the combined organic layers were washed with water. After drying over anhydrous magnesium sulfate and the desiccant was removed by filtration; the filtrate was then concentrated under reduced pressure. The resulting residue was purified by silica gel column chromatography (n-hexane:ethyl acetate=100:0-90:10) to give the titled compound as a colorless oil (510 mg).

1. stirringafter stirring the mixture at that temperature for 20 minutes
2. customto room temperature
3. extractiontwo extractions
4. washthe combined organic layers were washed with water
5. dry with materialAfter drying over anhydrous magnesium sulfate
6. customthe desiccant was removed by filtration
7. concentrationthe filtrate was then concentrated under reduced pressure
8. customThe resulting residue was purified by silica gel column chromatography (n-hexane:ethyl acetate=100:0-90:10)

ORD-Eintrag

ord-e0350786af7147eab5fffba7ba6000bb

Quelldatensatz

uspto-grants-2016_08

DOI

10.6084/m9.figshare.5104873.v1

Patentnummer

US09422240B2