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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2173665Generated: October 31, 2026

Chloroacetonitrile → HCID 671500, compound

https://huagongshe.com/reaction/2173665

Reaction equation

Participants

RoleNameHCIDCharge
ReactantChloroacetonitrileHCID 7856—
ReactantPotassium HydroxideHCID 14797—
Reactant5-chloro-4,6-dimethyl-2-sulfanylidene-1H-pyridine-3-carbonitrileHCID 11564661—
SolventDimethylformamideHCID 6228—
ProductHCID 671500HCID 67150086.4%

Reaction Steps

The 5-chloro-4,6-dimethyl-2-thioxo-1,2-dihydropyridine-3-carbonitrile (300 mg, 1.51 mmol) was stirred in the DMF (3.0 mL). An aqueous solution of 10% KOH (0.85 mL, 1.51 mmol) was added, followed by chloroacetonitrile (0.095 mL, 1.51 mmol). The reaction was stirred at RT for 15 minutes, LC/MS indicates initial thio-alkylation is complete. A second equivalent of 10% KOH (0.85 mL, 1.51 mmol) was added and the resulting slurry was warmed to 50° C. and stirred about 30 min. LC/MS indicates reaction is done. The slurry was cooled to RT, then poured into 50 g of crushed ice and allowed to warm until the ice melted. The cold slurry was poured through filter paper, washing the solid with cold water. The solid was collected and dried in a vacuum oven at 60° C. to give 310 mg (86%) of the pure product as a light yellow solid. 1H NMR (400 MHz, DMSO-d6): δ ppm 6.56 (s, 1H), 2.80 (s, 3H), 2.62 (s, 3H). LC/MS: RT=0.73 min., m/z=238.0 [M+H]+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09056876B2
Source datasetuspto-grants-2015_06
ORD IDord-3064fdf81d264db48a9c6909de41f20d
Source noteuspto-grants-2015_06