Water → 2-(2-Chloro-4-fluoro-phenyl)-3-oxo-butyronitrile

Temperature

70 °C

A suspension of dry, solid sodium ethoxide (Aldrich, 10.2 g, 150 mmol) in a mixture of xylenes (60 mL) and anhydrous ethanol (25 mL) was stirred at 70° C., and a solution of 2-chloro-4-fluorobenzeneacetonitrile (16.96 g, 100 mmol) in a mixture of ethyl acetate (30 mL) and ethanol (5 mL) was added dropwise to the hot reaction mixture over 20 minutes. The reaction mixture was heated at 75-78° C. for 3 h and then allowed to cool. Water (50 mL) was added to dissolve solids. The mixture was extracted once with ethyl acetate, and the extract was discarded. The aqueous phase was acidified to pH 2 by addition of 1 N aqueous hydrochloric acid, and then extracted with ethyl acetate (50 mL). The ethyl acetate phase was dried (MgSO4) and evaporated to provide the intermediate product α-acetyl-2-chloro-4-fluorobenzeneacetonitrile as a solid (14.8 g).

1. additionA suspension
2. customof dry
3. additionwas added dropwise to the hot reaction mixture over 20 minutes
4. temperatureThe reaction mixture was heated at 75-78° C. for 3 h
5. temperatureto cool
6. dissolutionto dissolve solids
7. extractionThe mixture was extracted once with ethyl acetate
8. additionThe aqueous phase was acidified to pH 2 by addition of 1 N aqueous hydrochloric acid
9. extractionextracted with ethyl acetate (50 mL)
10. dry with materialThe ethyl acetate phase was dried (MgSO4)
11. customevaporated

ORD record

ord-84422eb2c4ff46068a4e7a9cc1ebddb8

Source dataset

uspto-grants-2015_08

DOI

10.6084/m9.figshare.5104873.v1

Patent number

US09107412B2