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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1720587Generated: October 27, 2026

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

https://huagongshe.com/reaction/1720587

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 numberUS05506242
Source datasetuspto-grants-1996_04
ORD IDord-7ebbe66aebb04a53b2d5ddf9183a29cf
Source noteuspto-grants-1996_04