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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1646271Generated: October 30, 2026

Pyridine → HCID 19801956, compound

https://huagongshe.com/reaction/1646271

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPyridineHCID 1049—
ReactantCyclohexanethiolHCID 15290—
ReactantHCID 19801962HCID 19801962—
SolventTolueneHCID 1140—
SolventDiethyl EtherHCID 3283—
ProductHCID 19801956HCID 1980195666.2%

Reaction Steps

4.0 g of 4-chloro-4,4-difluorobutyryl chloride are added dropwise over the course of 30 minutes to a solution of 2.6 g of cyclohexyl mercaptan and 4.5 g of pyridine in 50 ml of toluene at 0° C. The reaction mixture is stirred at RT for 16 hours and then diluted with 150 ml of diethyl ether and subsequently washed with 50 ml each of 1N HCl, saturated NaHCO3 and saturated NaCl solution. The organic phase is then dried over MgSO4, filtered and evaporated. The resulting crude product is distilled at +90° C./5 mbar. 3.8 g of S-cyclohexyl 4-chloro-4,4-difluorothiobutyrate are obtained as an oil, nD23 : 1.4748.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05179121
Source datasetuspto-grants-1993_01
ORD IDord-32b64a4a66184f2286896be9ecab2987
Source noteuspto-grants-1993_01