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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1720581Generated: November 1, 2026

Benzyl Bromide → HCID 10647114, compound

https://huagongshe.com/reaction/1720581

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzyl BromideHCID 7498—
ReactantSodium hydrideHCID 24758—
ReactantN-[4-methoxybenzenesulfonyl]-(D)-leucine t-butyl esterHCID 10808269—
SolventDimethylformamideHCID 6228—
ProductHCID 10647114HCID 10647114—

Reaction Steps

To a suspension of sodium hydride (0.68 g, 14.1 mmol) in dimethylformamide (60.0 mL), is added N-[4-methoxybenzenesulfonyl]-(D)-leucine t-butyl ester (5.02 g, 14.06 mmol) in dimethylformamide (10.0 mL). After stirring at room temperature for 20 minutes, benzyl bromide (1.67 mL, 14.06 mmol) is added, and the reaction is stirred overnight at room temperature. The reaction is then partitioned between ethyl acetate and acidic water (pH=5), the organic layer is dried (Na2SO4), and the solvent is evaporated. The product is purified by silica gel chromatography (10% ethyl acetate/hexane) to give t-butyl 2(R)-[[4-methoxybenzenesulfonyl](benzyl)amino]-4-methylpentanoate.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05506242
Source datasetuspto-grants-1996_04
ORD IDord-2e5b236b4f094377899f7fb4f58ae54f
Source noteuspto-grants-1996_04