Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1859727Generated: November 3, 2026

Benzenesulfonyl chloride → HCID 53909776, compound

https://huagongshe.com/reaction/1859727

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzenesulfonyl chlorideHCID 7369—
Reactant3-Amino-4-methoxybenzanilideHCID 8426—
ReactantTriethylamineHCID 8471—
SolventEthyl AcetateHCID 8857—
ProductHCID 53909776HCID 5390977617.5%

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 ½ 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 numberUS06528528B2
Source datasetuspto-grants-2003_03
ORD IDord-fe9fcc0e43be4511a3e2018857990a26
Source noteuspto-grants-2003_03