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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1604683Generated: October 31, 2026

Thionyl Chloride → HCID 19603735, compound

https://huagongshe.com/reaction/1604683

Reaction equation

Participants

RoleNameHCIDCharge
ReactantThionyl ChlorideHCID 24386—
ReactantHCID 19603770HCID 19603770—
SolventChloroformHCID 6212—
ProductHCID 19603735HCID 19603735—

Reaction Steps

A mixture of 1-{[2-(4-tert-butylthiazol-2-yl)benzofuran-5-yl]methyl}-5-(hydroxymethyl)indole-3-carbonitrile (0.66 g) and thionyl chloride (0.5 ml) in chloroform (20 ml) was stirred at room temperature for 3 hours. After neutralization with aqueous sodium hydrogen carbonate, the resulting mixture was extracted with chloroform. The organic layer was washed with water and brine, dried over magnesium sulfate and evaporated under reduced pressure to give 1-{[2-(4-tert-butylthiazol-2-yl)benzofuran-5-yl]methyl}-5-(chloromethyl)indole-3-carbonitrile (0.67 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05994378
Source datasetuspto-grants-1999_11
ORD IDord-bc6a215c286841cc851fffda0733992d
Source noteuspto-grants-1999_11