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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 433334Generated: October 29, 2026

Pyridine → HCID 18758697, compound

https://huagongshe.com/reaction/433334

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPyridineHCID 1049—
ReactantEthylene carbonateHCID 7303—
Reactant4'-MercaptoacetanilideHCID 70777—
Reactant3-Chloro-4-acetamidobenzene-1-sulfonyl chlorideHCID 282749—
ReactantSodium ethoxideHCID 2723922—
Catalyst4-(Dimethylamino)pyridineHCID 14284—
SolventEthanolHCID 702—
SolventDichloromethaneHCID 6344—
ProductHCID 18758697HCID 1875869719.3%

Reaction Steps

A solution of 4-acetamidothiophenol (8.35 g, 50.0 mmol), ethylene carbonate (5.5 g, 62.5 mmol) and sodium ethoxide (4.1 g, 60.0 mmol) in ethanol (250 ml) was heated at reflux overnight and then cooled to ambient temperature and evaporated to dryness. The residue was dissolved in diethyl ether (500 ml), washed with 1M aqueous hydrochloric acid and brine, dried and evaporated to dryness. The residue was dissolved in ethanol (120 ml) and 2M aqueous sodium hydroxide (60 ml) was added. The mixture was heated at reflux overnight and then cooled to ambient temperature and evaporated to dryness. Water (25 ml) was added to the residue and the solution was neutralised to pH 7 by the addition of 1M aqueous hydrochloric acid. The aqueous solution was extracted with EtOAc, the EtOAc extracts were washed with brine, dried and evaporated to dryness. The residue was dissolved in DCM (100 ml) and added to a solution of 4-acetamido-3-chlorobenzenesulphonyl chloride (5.5 g, 20.5 mmol), 4-dimethylaminopyridine (50 mg, 0.4 mmol) and pyridine (5.0 ml, 60 mmol) in DCM (100 ml). The mixture was stirred at ambient temperature overnight, the solution was evaporated to dryness, the residue dissolved in diethyl ether (450 ml), washed with 1M aqueous hydrochloric acid and brine, dried and evaporated to dryness. The residue was dissolved in ethanol (100 ml) and 2M aqueous sodium hydroxide (25 ml) was added. The mixture was heated at reflux overnight and then cooled to ambient temperature and evaporated to dryness. Water (25 ml) was added to the residue and the solution was neutralised to pH 7 by the addition of 1M aqueous hydrochloric acid. The aqueous solution was extracted with EtOAc, the EtOAc extracts were washed with brine, dried and evaporated to dryness. The residue was purified by column chromatography using 10% EtOAc in DCM to yield the title compound (1.53 g, 3.96 mmol). NMR: 1.0 (t, 3H), 3.0 (t, 2H), 3.3-3.5 (m, 4H), 6.2 (s, 2H), 6.75 (d, 1H), 7.0 (d, 2H), 7.2 (d, 2H), 7.3 (dd, 1H), 7.45 (d, 1H); MS: 385.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06667342B1
Source datasetuspto-grants-2003_12
ORD IDord-b1fc78bb557043a187c43057e06c517e
Source noteuspto-grants-2003_12