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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1763685Generated: October 30, 2026

Pyridine → N-(Phenylsulfonyl)glycine Methyl Ester

https://huagongshe.com/reaction/1763685

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPyridineHCID 1049—
ReactantBenzenesulfonyl chlorideHCID 7369—
ReactantGlycine methyl ester hydrochlorideHCID 122755—
SolventWaterHCID 962—
SolventDichloromethaneHCID 6344—
ProductN-(Phenylsulfonyl)glycine Methyl EsterHCID 514928853.1%

Reaction Conditions

Temperature25 °C

Reaction Steps

A 47.5 g (0.6 mol) sample of pyridine was added dropwise to a stirred and cooled (ice bath) slurry of 53.0 g (0.3 mol) benzenesulfonyl chloride and 37.7 g (0.3 mol) glycine methyl ester hydrochloride in 500 ml dichloromethane. The reaction mixture was then allowed to warm to 25° C. and was stirred for about 16 hours. The reaction mixture was diluted with 250 ml water, the organic layer was separated, washed with water, washed with 10% aqueous hydrochloric acid solution, washed with water, dried over magnesium sulfate and evaporated to give 36.5 g N-(methoxycarbonylmethyl)benzenesulfonamide, which crystallized as a colorless solid melting at 62°-63° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04112237
Source datasetuspto-grants-1978_09
ORD IDord-84bc3a3349a8481bb7679bc05e60f6e6
Source noteuspto-grants-1978_09