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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 491859Generated: October 30, 2026

Benzenesulfonyl chloride, 3,4-dichloro- → HCID 57678944, compound

https://huagongshe.com/reaction/491859

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzenesulfonyl chloride, 3,4-dichloro-HCID 7383—
ReactantPotassium HydroxideHCID 14797—
ReactantHCID 57678947HCID 57678947—
CatalystTetrabutylammonium hydrogen sulfateHCID 94433—
SolventDichloromethaneHCID 6344—
ProductHCID 57678944HCID 57678944—

Reaction Steps

To a dry round bottom flask, (5-Methoxy-1H-indol-3-ylsulfanyl)-acetic acid methyl ester (25, 7.0 mg, 0.027 mmol) was dissolved with CH2Cl2 (3.0 mL). Tetrabutylammonium hydrogen sulfate (2.0 mg) and 50% KOH solution (3.0 mL) were added next. After about 5 minutes of stirring, 3,4-dichloro-benzenesulfonyl chloride (20 mg, 0.081 mmol) was added. This reaction was allowed to stir at ambient temperature overnight. The reaction was extracted with dichloromethane (2×14 mL), washed with water (5 mL), brine (5 mL) and dried over anhydrous magnesium sulfate. The reactant was filtered and rotoevaporated to give the desired product 26 as off white solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07531568B2
Source datasetuspto-grants-2009_05
ORD IDord-46a6736ce26f48cf8f7f00dc55bf1ce6
Source noteuspto-grants-2009_05