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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2303352Generated: October 26, 2026

Triethylamine → Methyl 2-(2-nitrobenzenesulfonamido)acetate

https://huagongshe.com/reaction/2303352

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
Reactant2-Nitrobenzenesulfonyl chlorideHCID 15540—
ReactantGlycine methyl ester hydrochlorideHCID 122755—
SolventDichloromethaneHCID 6344—
ProductMethyl 2-(2-nitrobenzenesulfonamido)acetateHCID 743502—

Reaction Steps

Glycine methyl ester hydrochloride (15.0 g) was dissolved in dichloromethane, and to the solution triethylamine (26.48 g) was added at 0° C. A solution of 2-nitrobenzenesulfonyl chloride (23.57 g) in dichloromethane (50 mL) was then gradually added dropwise. After the mixture was stirred at room temperature for 2 hours, the reaction mixture was concentrated under reduced pressure, and ethyl acetate was added to the residue. The resultant mixture was washed with 2 M hydrochloric acid, water and saturated brine, dried over anhydrous sodium sulfate and concentrated under reduced pressure. The resultant crystals were recrystallized from ethyl acetate-hexane to obtain the title compound.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06432957B1
Source datasetuspto-grants-2002_08
ORD IDord-0d55c04c6ee34aff8cfdaeb4d1f92daa
Source noteuspto-grants-2002_08