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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1366935Generated: October 31, 2026

Pyridine → Ethyl 2-(4-methylphenylsulfonamido)acetate

https://huagongshe.com/reaction/1366935

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPyridineHCID 1049—
Reactant4-Toluenesulfonyl chlorideHCID 7397—
ReactantGlycine ethyl ester, hydrochlorideHCID 2723640—
SolventDichloromethaneHCID 6344—
ProductEthyl 2-(4-methylphenylsulfonamido)acetateHCID 23068596.4%

Reaction Steps

Tosyl chloride (14.75 g, 77.37 mmol) was added to a stirring mixture of glycine ethyl ester hydrochloride (9.0 g, 64.48 mmol) and pyridine (11.45 mL, 141.85 mmol) in 100 mL of dichloromethane. After stirring overnight, the mixture was washed with water and dilute NaOH. The combined organics were dried with Na2SO4, filtered, evaporated under reduced pressure to give 16.0 g (96%) of 81, which was used without purification in the next reaction. 1H-NMR (400 MHz, CDCl3): δ 1.18 (t, 3H), 2.42 (s, 3H), 3.76 (d, 2H), 4.08 (q, 2H), 5.22 (m, 1H), 7.30 (d, 2H), 7.75 (d, 2H) ppm. 13C-NMR (100 MHz, CDCl3): δ 13.99, 21.55, 44.19, 61.89, 127.28, 129.76, 136.20, 143.81, 168.87 ppm. □ DEPT (100 MHz, CDCl3): CH3 carbons: 13.99, 21.55; CH2 carbons: 44.19, 61.89; CH carbons: 127.28, 129.76 ppm. LC/MS: 95%, m/z=257.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07893098B2
Source datasetuspto-grants-2011_02
ORD IDord-4209087824684f1eba008f684431184f
Source noteuspto-grants-2011_02