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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1720608Generated: October 29, 2026

Ethyl bromoacetate → Ethyl 2-[[4-methoxybenzenesulfonyl](benzyl)amino]acetate

https://huagongshe.com/reaction/1720608

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl bromoacetateHCID 7748—
ReactantSodium hydrideHCID 24758—
ReactantN-benzyl-4-methoxybenzenesulfonamideHCID 741351—
SolventTetrahydrofuranHCID 8028—
ProductEthyl 2-[[4-methoxybenzenesulfonyl](benzyl)amino]acetateHCID 3503631—

Reaction Steps

Sodium hydride (1.56 g of a 50 % oil dispersion, 33.0 mmol) is suspended in tetrahydrofuran (85 mL). To this is added a solution of N-[4-methoxybenzenesulfonyl]-benzylamine (9.0 g, 32.5 mmol) also in tetrahydrofuran (85 mL), and the reaction is stirred for 30 minutes at room temperature. Then ethyl bromoacetate (5.40 mL, 48.8 mmol) is added, and the reaction is stirred overnight at room temperature. The reaction is quenched with a small amount of water, and all the solvent is removed. The crude mixture is partitioned between ethyl acetate and water, the aqueous phase is extracted several times with ethyl acetate, the combined organic layers are dried (Na2SO4), and the solvent is evaporated. The product is purified by silica gel chromatography (30% ethyl acetate/hexane) to give ethyl 2-[[4-methoxybenzenesulfonyl](benzyl)amino]acetate.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05506242
Source datasetuspto-grants-1996_04
ORD IDord-012d7995ce6b4e019f89346dc5b649b9
Source noteuspto-grants-1996_04