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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1604642Generated: October 31, 2026

Thionyl Chloride → HCID 19603774, compound

https://huagongshe.com/reaction/1604642

Reaction equation

Participants

RoleNameHCIDCharge
ReactantThionyl ChlorideHCID 24386—
ReactantSodium BicarbonateHCID 516892—
ReactantHCID 19603716HCID 19603716—
Solvent1,2-DichloroethaneHCID 11—
ProductHCID 19603774HCID 19603774—

Reaction Steps

A mixture of 4-tert-butyl-2-[5-(1-hydroxyethyl)-benzofuran-2-yl]thiazole (1.5 g) and thionyl chloride (0.44 ml) in 1,2 dichloroethane (35 ml) was stirred under reflux for 2 hours. After cooling, the resulting mixture was adjusted to pH 7 with aqueous sodium hydrogen carbonate solution. The organic layer was separated, washed with brine, dried over magnesium sulfate and evaporated under reduced pressure to give 4-tert-butyl-2-[5-(1-chloroethyl)-benzofuran-2-yl]thiazole (1.31 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05994378
Source datasetuspto-grants-1999_11
ORD IDord-9891fd7f53e441efb41423b75583ac45
Source noteuspto-grants-1999_11