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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2086225Generated: October 27, 2026

Ethyl bromoacetate → N-(2,2-dimethoxyethyl)-N-(6-chloro-2-naphthalenesulfonyl)glycine ethyl ester

https://huagongshe.com/reaction/2086225

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl bromoacetateHCID 7748—
ReactantSodium hydrideHCID 24758—
ReactantN-(2,2-dimethoxyethyl)-6-chloro-2-naphthalenesulfonamideHCID 22727126—
SolventDimethylformamideHCID 6228—
SolventTetrahydrofuranHCID 8028—
ProductN-(2,2-dimethoxyethyl)-N-(6-chloro-2-naphthalenesulfonyl)glycine ethyl esterHCID 22727098—

Reaction Conditions

Temperature0 °C

Reaction Steps

N-(2,2-Dimethoxyethyl)-6-chloro-2-naphthalenesulfonamide was dissolved in DMF (100 ml) and combined with sodium hydride (1.16 g, in oil), cooled to 0° C., treated dropwise with a solution of ethyl bromoacetate (4.843 g) in tetrahydrofuran (15 ml) and then stirred at room temperature for 3 hours. The reaction mixture was concentrated and the residue was dissolved in ethyl acetate, washed with water, aqueous sodium bicarbonate and brine, dried and concentrated to obtain N-(2,2-dimethoxyethyl)-N-(6-chloro-2-naphthalenesulfonyl)glycine ethyl ester as a colorless oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06723722B1
Source datasetuspto-grants-2004_04
ORD IDord-0e14b0866fcb4b4389a2b91efa991a48
Source noteuspto-grants-2004_04