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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1492544Generated: October 30, 2026

Triethylamine → 4-Chlorobenzenesulfonamide

https://huagongshe.com/reaction/1492544

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
ReactantEthyl chloroformateHCID 10928—
ReactantHCID 18950677HCID 18950677—
SolventTetrahydrofuranHCID 8028—
Product4-ChlorobenzenesulfonamideHCID 66824—

Reaction Steps

A portion of 53 mg of N-[2-(4-hydroxyphenyl)-3-(3-pyridyl)propyl]-4-chlorobenzenesulfonamide and 78 mg of triethylamine were dissolved in 8 ml of tetrahydrofuran, followed by addition of 25 mg of ethyl chlorocarbonate dissolved in 1 ml of tetrahydrofuran, and stirred at room temperature for 10 minutes. The crystalline deposited was filtered, and the filtrate was then concentrated under reduced pressure. The residue was subjected to chromatography on a silica gel column, and from a fraction eluted with methanol-methylene chloride (5:95 v/v) was obtained 53 mg of N-[2-(4-ethoxycarbonyloxyphenyl)-3-(3-pyridyl)}propyl]-4-chlorobenzenesulfonamide. The spectrometric data supports the structure of [32] as follows.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05374641
Source datasetuspto-grants-1994_12
ORD IDord-79ee0d75002f4f1faea4c11dec357b22
Source noteuspto-grants-1994_12