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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1088734Generated: October 27, 2026

Hydrochloric Acid → Pyridin-3-yl(2-(trifluoromethyl)phenyl)methanone

https://huagongshe.com/reaction/1088734

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantDiethyl EtherHCID 3283—
Reactant3-BromopyridineHCID 12286—
Reactant2-(Trifluoromethyl)benzonitrileHCID 67972—
ReactantButyllithiumHCID 178418339—
SolventHexaneHCID 8058—
ProductPyridin-3-yl(2-(trifluoromethyl)phenyl)methanoneHCID 1482033763%

Reaction Steps

To a stirred and cooled (-70°~-80° C.) solution of 71.4 parts of a 1-butyllithium solution 1.6M in hexane in 105 parts of 1,1'-oxybisethane was added dropwise a solution of 40.6 parts of 3-bromopyridine in 70 parts of 1,1'-oxybisethane. Upon complete addition, stirring was continued for 15 minutes and a solution of 30 parts of 2-(trifluoromethyl)benzonitrile in 35 parts of 1,1'-oxybisethane was added dropwise at this low temperature. Upon completion, the mixture was stirred for 3 hours at this low temperature. The mixture was heated to room temperature and poured into 84 parts of a hydrochloric acid solution 10N and some crushed ice. The aqueous layer was separated and heated to the boiling point. After cooling, the mixture was made alkaline with an ammonium hydroxide solution and the product was extracted with dichloromethane. The extract was dried, filtered and concentrated. The residue was purified by filtration over silica gel using trichloromethane as eluent. The pure fractions were collected and the eluent was concentrated, yielding 27.8 parts (63%) of (3-pyridinyl) [2-(trifluoromethyl)phenyl]methanone as an oily residue (intermediate 3).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04963573
Source datasetuspto-grants-1990_10
ORD IDord-79d1b002ff4349e78e8055309b913ab0
Source noteuspto-grants-1990_10