Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2226210Generated: October 30, 2026

Water → 3,4-dichlorobenzenesulfonamide

https://huagongshe.com/reaction/2226210

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantBenzenesulfonyl chloride, 3,4-dichloro-HCID 7383—
ReactantSodium HydroxideHCID 14798—
ReactantHCID 9998338HCID 9998338—
SolventPyridineHCID 1049—
Product3,4-dichlorobenzenesulfonamideHCID 233097—

Reaction Steps

To a solution of 3,4-dichlorobenzenesulfonyl chloride (1.84 g, 7.5 mmol) in 35 mL of dry pyridine was added 2.5 g (7 mmol) of 4-(aminomethyl)-1-[[2-(diethylamino)ethyl]amino]-thioxanthen-9-one (prepared by the method described in Example 4) under nitrogen and the reaction mixture was stirred at room temperature for 15 min. and then was allowed to stand for approximately 72 hours. The reaction mixture was poured into 75 mL of water containing 0.75 g of NaOH, and extracted into chloroform. The organic layer was washed with water (2x) and brine, and dried over sodium sulfate. Chloroform was removed in vacuo, the residue was recrystallized from ethanol to afford 1.24 g of N-[[1-[[2-(diethylamino)]ethyl]amino]-9-oxothioxanthen-4-yl]methyl]-3,4-dichlorobenzenesulfonamide, m.p. 95° C. (dec.). The free base was dissolved in methanol and treated with methanesulfonic acid in methanol to afford the methanesulfonate.1/2 hydrate, m.p. 55° C. (dec.).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05346917
Source datasetuspto-grants-1994_09
ORD IDord-e30c296168424ac0b991a93d914db9ea
Source noteuspto-grants-1994_09