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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1701893Generated: October 27, 2026

Water → 2-(Pyrid-2-yl)-tetrahydrothiopyran

https://huagongshe.com/reaction/1701893

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantHexamethylphosphoramideHCID 12679—
ReactantPyrid-2-ylmethyl 4-chlorobutyl sulphideHCID 9990871—
ReactantPotassium tert-butoxideHCID 23665647—
SolventDiethyl EtherHCID 3283—
SolventTetrahydrofuranHCID 8028—
Product2-(Pyrid-2-yl)-tetrahydrothiopyranHCID 1372063474.3%

Reaction Steps

A solution of pyrid-2-ylmethyl 4-chlorobutyl sulphide (82 g) in anhydrous tetrahydrofuran (100 cc) is added dropwise, in the course of 15 minutes and whilst keeping the temperature below 30° C., to a solution of potassium tert.-butoxide (66 g) in a mixture of anhydrous hexamethylphosphorotriamide (100 cc) and anhydrous tetrahydrofuran (530 cc). After stirring for 1 hour at a temperature of about 20° C., potassium tert.-butoxide (20 g) is added and stirring is continued for 45 minutes at the same temperature. The reaction mixture is added to a mixture of distilled water (1000 cc) and diethyl ether (600 cc); after decantation, the aqueous phase is extracted twice with diethyl ether (400 cc in total). The ether extracts are combined, washed three times with distilled water (3000 cc in total), dried over anhydrous sodium sulphate and filtered and the filtrate is concentrated under reduced pressure (20 mm Hg; 2.7 kPa) at 35° C. 2-(Pyrid-2-yl)-tetrahydrothiopyran (50.6 g) is thus obtained in the form of a brown oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04379154
Source datasetuspto-grants-1983_04
ORD IDord-b2344d1fc0184ddf9c2a88c5098e9428
Source noteuspto-grants-1983_04