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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 264293Generated: October 27, 2026

Benzyl Bromide → Methyl 2-[[4-methoxybenzenesulfonyl](benzyl)amino]propionate

https://huagongshe.com/reaction/264293

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzyl BromideHCID 7498—
ReactantSodium hydrideHCID 24758—
ReactantN-[4-methoxybenzenesulfonyl]-alanine methyl esterHCID 7081982—
SolventDimethylformamideHCID 6228—
ProductMethyl 2-[[4-methoxybenzenesulfonyl](benzyl)amino]propionateHCID 22907154—

Reaction Steps

To a suspension of sodium hydride (0.60 g, 11.0 mmol) in dimethylformamide (20.0 mL), is added N-[4-methoxybenzenesulfonyl]-alanine methyl ester (2.6 g, 10.0 mmol) in dimethylformamide (10.0 mL). After stirring at room temperature for 30 minutes, benzyl bromide (1.22 mL, 10.0 mmol) is added, and the reaction is stirred for two hours at room temperature. The reaction is then partitioned between ether and brine, the organic layer is dried (Na2SO4), and the solvent is evaporated. The product is purified by silica gel chromatography (20% ether/hexanes) to give methyl 2-[[4-methoxybenzenesulfonyl]-(benzyl)amino]-propionoate.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05646167
Source datasetuspto-grants-1997_07
ORD IDord-c9a5b98f988f4afc8ad6f62b26af50be
Source noteuspto-grants-1997_07