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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2113446Generated: October 26, 2026

Triethylamine → 2-Fluoro-5-(trifluoromethoxy)benzonitrile

https://huagongshe.com/reaction/2113446

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
ReactantTrifluoroacetic anhydrideHCID 9845—
Reactant(NE)-N-[[2-fluoro-5-(trifluoromethoxy)phenyl]methylidene]hydroxylamineHCID 87441576—
SolventTetrahydrofuranHCID 8028—
Product2-Fluoro-5-(trifluoromethoxy)benzonitrileHCID 522109583%

Reaction Steps

To a solution of E-2-fluoro-5-trifluoromethoxy-benzaldehyde oxime (47.5 g, 213 mmol) in THF (400 ml) was added triethylamine (65.0 ml, 466 mmol). The mixture was cooled in an ice bath and trifluoroacetic anhydride (32.8 ml, 236 mmol) was added at such a rate that the temperature was kept <30° C. After 1 h at rt all volatiles were evaporated (40° C., 200 mbar). The oily residue was partitioned (ether/water), the organic phase was dried (Na2SO4) and concentrated. Distillation (24 mbar, T=80-83° C.) afforded the title compound (36.1 g, 83%) that was sufficiently pure to be used in the next step. MS: m/e=205 [M]+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07432256B2
Source datasetuspto-grants-2008_10
ORD IDord-855596fb52db41159cd658ec321a7dd1
Source noteuspto-grants-2008_10