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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 868301Generated: October 25, 2026

Potassium Hydroxide → 2-(4-Fluorophenyl)propanenitrile

https://huagongshe.com/reaction/868301

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium HydroxideHCID 14797—
ReactantBenzeneacetonitrile, 4-fluoro-HCID 68016—
ReactantSodium MethoxideHCID 10942334—
ReactantCID 21226545HCID 21226545—
SolventWaterHCID 962—
SolventIsopropanolHCID 3776—
SolventO-XyleneHCID 7237—
Product2-(4-Fluorophenyl)propanenitrileHCID 103573—

Reaction Steps

A mixture of 68 parts of 4-fluorobenzeneacetonitrile, 180 parts of ethyl carbonate, 100 parts of a sodium methoxide solution 30% and 200 parts of dimethylbenzene was distilled till an internal temperature of 110° C. was reached. The distillate was cooled and 80 parts of 2-propanol were added, followed by the dropwise addition of 63 parts of methyl sulfate at room temperature (exothermic reaction: temperature rose to 80° C.). The remaining 120 parts of 2-propanol were added while stirring vigorously. Upon completion, stirring was continued for 20 hours. Then there were added 56 parts of potassium hydroxide (exothermic reaction: temperature rose to 75° C.). The whole was stirred and refluxed for 30 minutes. The reaction mixture was cooled and poured into 750 parts of water. The aqueous phase was separated and extracted with methylbenzene. The extract was dried, filtered and evaporated. The oily residue was distilled, yielding 54 parts of 4-fluoro-α-methylbenzeneacetonitrile; bp. 110°- 115° C. at 11 mm. pressure (intermediate 1).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04778887
Source datasetuspto-grants-1988_10
ORD IDord-5c732eb0904b45989b9c5a1c88932afc
Source noteuspto-grants-1988_10