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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1387569Generated: October 31, 2026

Benzenesulfonyl chloride → HCID 21715919, compound

https://huagongshe.com/reaction/1387569

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzenesulfonyl chlorideHCID 7369—
Reactant3-Amino-4-methoxybenzanilideHCID 8426—
ReactantTriethylamineHCID 8471—
ReactantEthyl AcetateHCID 8857—
ProductHCID 21715919HCID 21715919—

Reaction Steps

A mixture of 3-amino-4-methoxy-N-phenyl-benzamide (0.9726 g, 4.00 mmol), triethylamine (0.56 mL, 4.02 mmol), and benzenesulfonyl chloride (0.51 mL, 4.00 mmol) in ethyl acetate (70 mL) was heated briefly to obtain a solution. The reaction was stirred overnight at room temperature under nitrogen. An additional equivalent of triethylamine and 1/2 equivalent of benzenesulfonyl chloride was added and the mixture heated to 50-60° C. After 7 hours, the solvent was removed in vacuo and the residue dissolved in ethyl acetate and washed with 1N HCl followed by saturated NaHCO3. The organic layer was filtered, dried with MgSO4, and stripped of solvent by rotary evaporator. Trituration of the residue in hexane/ethyl acetate (4:1) afforded the product (0.268 g); m.p. 190-194° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06268387B1
Source datasetuspto-grants-2001_07
ORD IDord-87b391f93cc340368e1fdfa2a8da9ea4
Source noteuspto-grants-2001_07