HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 894330Generated: October 30, 2026
Pyridine → N-(Phenylsulfonyl)glycine Methyl Ester
https://huagongshe.com/reaction/894330
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Pyridine | HCID 1049 | — |
| Reactant | Benzenesulfonyl chloride | HCID 7369 | — |
| Reactant | Glycine methyl ester hydrochloride | HCID 122755 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | N-(Phenylsulfonyl)glycine Methyl Ester | HCID 5149288 | 53.1% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04283416 |
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| Source dataset | uspto-grants-1981_08 |
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| ORD ID | ord-268212491fbe4db9a3fb80ad7e46ffa3 |
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| Source note | uspto-grants-1981_08 |
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