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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2164158Generated: October 31, 2026

Chlorotrimethylsilane → HCID 22750284, compound

https://huagongshe.com/reaction/2164158

Reaction equation

Participants

RoleNameHCIDCharge
ReactantChlorotrimethylsilaneHCID 6397—
ReactantTetrahydrofuranHCID 8028—
ReactantThionyl ChlorideHCID 24386—
ReactantHCID 22750277HCID 22750277—
SolventTriethylamineHCID 8471—
ProductHCID 22750284HCID 22750284—

Reaction Steps

A stirred suspension of 2.6 g. of 6-[3-(aminosulfonyl)phenyl]-1,2-dihydro-2-oxonicotinic acid in 130 ml. of tetrahydrofuran is treated with 1.24 ml. of triethylamine. After a few minutes, the resulting solution is treated with 1.12 ml. of trimethylsilyl chloride and stirred 1 hour at room temperature. The solution is then treated with 1.28 ml. of thionyl chloride and stirred for 2 hours at room temperature. The resulting solution is diluted with 200 ml. of hexane and the precipitate of 6-[3-aminosulfonyl)phenyl]-1,2-dihydro-2-oxonicotinyl chloride is collected by filtration, washed with hexane and dried. The acid chloride is used as such without further purification.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04137408
Source datasetuspto-grants-1979_01
ORD IDord-7a9aed1df534428d8c32f6a75a296943
Source noteuspto-grants-1979_01