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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2100683Generated: October 31, 2026

Sodium Chloride → [3-Chloro-5-(trifluoromethyl)pyridin-2-yl]acetonitrile

https://huagongshe.com/reaction/2100683

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium ChlorideHCID 5234—
ReactantDichloromethaneHCID 6344—
ReactantHCID 49757460HCID 49757460—
SolventDimethyl SulfoxideHCID 679—
SolventWaterHCID 962—
Product[3-Chloro-5-(trifluoromethyl)pyridin-2-yl]acetonitrileHCID 16227272—

Reaction Conditions

Temperature160 °C

Reaction Steps

314 g (1.13 mol, 1 eq.) of methyl [3-chloro-5-(trifluoromethyl)-2-pyridinyl]-(cyano)acetate and 22 g (0.38 mol, 0.33 eq.) of sodium chloride are dissolved in a solution of 44 mL of water and 1.1 L of dimethyl sulphoxide. The reaction medium is stirred and heated at 160° C. Once all gas has been given off, the medium is cooled to ambient temperature. 1 L of water and 0.5 L of dichloromethane are added. After separation, the aqueous phase is extracted twice with 0.5 L of dichloromethane. The organic phase is washed twice with 0.5 L of water and dried over magnesium sulphate. After concentration, the crude product is diluted in 100 mL of dichloromethane and eluted with an ethyl acetate/heptane mixture (20/80) on a bed of silica. The filtrate is concentrated so as to produce [3-chloro-5-(trifluoromethyl)-2-pyridinyl]acetonitrile.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07572818B2
Source datasetuspto-grants-2009_08
ORD IDord-bb2033ece0894bc79ffa8328645415da
Source noteuspto-grants-2009_08