Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 34977Generated: October 29, 2026

Sulfuryl chloride → HCID 178439678, compound

https://huagongshe.com/reaction/34977

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSulfuryl chlorideHCID 24648—
ReactantHCID 178439672HCID 178439672—
SolventTetrahydrofuranHCID 8028—
ProductHCID 178439678HCID 178439678—

Reaction Steps

A solution of 1.38 g. of 5-[4-(2-propyl-3-hydroxyphenoxy)butyl]-tetrazole in 25 ml. of tetrahydrofuran was cooled to -10° C. by means of an external alcohol-ice bath. One millimole of sulfuryl chloride was slowly added and the reaction mixture was stirred for one hour. The mixture was evaporated under reduced pressure and the residue was triturated with diethyl ether. The ether was evaporated and the residue was purified by reverse phase high pressure liquid chromatography. The appropriate fractions provided 42 mg. of the desired title product plus 92 mg. of the 2-propyl-3-hydroxy-6-chlorophenoxy isomer and a small amount of the 2-propyl-3-hydroxy-4,6-dichlorophenoxy compound.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04764521
Source datasetuspto-grants-1988_08
ORD IDord-340c8fdaad77471d99b281f109e27b91
Source noteuspto-grants-1988_08