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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1931365Generated: October 25, 2026

Water → 3-Pyridinecarbonitrile, 6-(chlorodifluoromethyl)-

https://huagongshe.com/reaction/1931365

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
Reactant3-(Dimethylamino)prop-2-enenitrileHCID 97497—
ReactantAmmonium AcetateHCID 517165—
Reactant4-Ethoxy-1-chloro-1,1-difluoro-3-butene-2-oneHCID 5796722—
SolventTolueneHCID 1140—
Product3-Pyridinecarbonitrile, 6-(chlorodifluoromethyl)-HCID 1094324741.1%

Reaction Conditions

Temperature100 °C

Reaction Steps

(3E)-1-Chloro-4-ethoxy-1,1-difluorobut-3-en-2-one (7.36 g, 40 mmol) was dissolved in dry toluene (40 mL) and treated with 3-dimethylaminoacrylonitrile (4.61 g, 48 mmol) at room temperature. The solution was heated at about 100° C. for 3.5 hr. The solvent was then removed under reduced pressure and the remaining mixture was re-dissolved in dimethyl formamide (DMF; 20 mL), treated with ammonium acetate (4.62 g, 60 mmol) and stirred at room temperature overnight. Water was added to the reaction mixture and the resulting mixture was extracted with ether-CH2CH2 (1:2, v/v) twice. The combined organic layer was washed with brine, dried, filtered and concentrated. The residue was purified on silica gel to give 3.1 g of 6-[chloro(difluoro)methyl]nicotinonitrile (A) as light colored oil in 41% yield. GC-MS: mass calcd for C7H3ClF2N2 [M]+ 188. Found 188.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08188292B2
Source datasetuspto-grants-2012_05
ORD IDord-55356535618a4eb08c6dbf33cd6b9f14
Source noteuspto-grants-2012_05