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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2209678Generated: November 1, 2026

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

https://huagongshe.com/reaction/2209678

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 numberUS05455258
Source datasetuspto-grants-1995_10
ORD IDord-cdf3f62043194e2eb6920c401eb9ec97
Source noteuspto-grants-1995_10