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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1720588Generated: November 2, 2026

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

https://huagongshe.com/reaction/1720588

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 numberUS05506242
Source datasetuspto-grants-1996_04
ORD IDord-08a8b6f35b9744a0bd3f0190fe54157b
Source noteuspto-grants-1996_04