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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1957251Generated: October 27, 2026

Sodium Hydroxide → 3-Chloro-2-(4-chloro-3-dimethylaminothiocarbonyloxyphenyl)-5-trifluoromethylpyridine

https://huagongshe.com/reaction/1957251

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium HydroxideHCID 14798—
ReactantSodium hydrideHCID 24758—
ReactantDimethylthiocarbamoyl chlorideHCID 27871—
Reactant3-Chloro-2-(4-chloro-3-hydroxyphenyl)5-trifluoromethylpyridineHCID 19068759—
SolventDimethylformamideHCID 6228—
Product3-Chloro-2-(4-chloro-3-dimethylaminothiocarbonyloxyphenyl)-5-trifluoromethylpyridineHCID 53944733—

Reaction Conditions

Temperature80 °C

Reaction Steps

A solution of 65.0 g of 3-chloro-2-(4-chloro-3-hydroxyphenyl)-5-trifluoromethylpyridine in 200 ml of dimethylformamide, and then 31.3 g of dimethylthiocarbamoyl chloride, were added dropwise to a suspension of 6.7 g of 80% sodium hydride in 300 ml of anhydrous dimethylformamide. The solution was stirred at 80° C. for one hour and then poured into 2.5 1 of 1% by weight sodium hydroxide solution. After extraction three times with 250 ml of tert-butyl methyl ether each time the combined organic phases were washed twice with 150 ml of water each time and then dried over sodium sulfate and concentrated until crystallization started. After removal of the crystals, the mother liquor was concentrated further until more of the product started to crystallized out.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05783522
Source datasetuspto-grants-1998_07
ORD IDord-33873b7af43944a18b7fe038a6690831
Source noteuspto-grants-1998_07