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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 742030Generated: October 30, 2026

4-Methoxybenzenesulfonyl chloride → N-[4-methoxybenzenesulfonyl]-alanine methyl ester

https://huagongshe.com/reaction/742030

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-Methoxybenzenesulfonyl chlorideHCID 7401—
ReactantTriethylamineHCID 8471—
ReactantSodium HydroxideHCID 14798—
ReactantAlanine methyl ester hydrochlorideHCID 2733257—
SolventDichloromethaneHCID 6344—
ProductN-[4-methoxybenzenesulfonyl]-alanine methyl esterHCID 7081982—

Reaction Steps

Alanine methyl ester hydrochloride (7.0 g, 50.0 mmol) is dissolved in methylene chloride (100.0 mL) and triethylamine (20.0 mL, 143.0 mmol). To this solution is added 4-methoxybenzenesulfonyl chloride (10.3 g, 50.0 mmol), and the reaction is stirred at room temperature briefly. The reaction is made basic with 1N sodium hydroxide, and washed with methylene chloride. The combined organic layers are dried (Na2SO4), and the solvent is evaporated. Hexane is added to the residue and the precipitate is collected to give N-[4-methoxybenzenesulfonyl]-alanine methyl ester.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05552419
Source datasetuspto-grants-1996_09
ORD IDord-18540110dc3b4178b4c9293ee2fdbfa8
Source noteuspto-grants-1996_09