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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2209679Generated: October 30, 2026

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

https://huagongshe.com/reaction/2209679

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 numberUS05455258
Source datasetuspto-grants-1995_10
ORD IDord-850f509113e14e31a7618c632424a5df
Source noteuspto-grants-1995_10