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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1164623Generated: November 1, 2026

4-Toluenesulfonyl chloride → HCID 13388351, compound

https://huagongshe.com/reaction/1164623

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-Toluenesulfonyl chlorideHCID 7397—
ReactantHCID 13388338HCID 13388338—
SolventPyridineHCID 1049—
ProductHCID 13388351HCID 1338835117%

Reaction Conditions

Temperature80 °C

Reaction Steps

Stirring a solution of diethyl 2-methyl-4-(2-chlorophenyl)-6-hydroxymethyl-1,4-dihydropyridine-3,5-dicarboxylate (1.1395 g) in dried pyridine (10 ml) at room temperature, a solution of p-toluenesulfonyl chloride (629.1 mg) in dried pyridine (10 ml) was dropwise added gradually thereto. The resultant mixture was stirred at room temperature for 1.5 hours and then heated at 80° C. for 4.5 hours with stirring. After removal of the pyridine, water was added to the residue and the resultant aqueous mixture was acidified with dil. hydrochloric acid and extracted twice with ethyl acetate. The extract was washed with dil. hydrochloric acid and then water, and dried. The resultant brown viscous oil was purified by column chromatography on silica-gel using an eluent (benzene:diethyl ether=1:1) to give an orange oil, which was crystallized by treating with diethyl ether. The resultant crystals were collected by filtratin and recrystallized from a mixture of diethyl ether and n-hexane to give orange-yellowish prisms (0.1926 g) of diethyl 2-methyl-4-(2-chlorophenyl)-6-formyl-1,4-dihydropyridine-3,5-dicarboxylate, m.p. 87° to 88° C., which was identified with an authentic sample.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04370334
Source datasetuspto-grants-1983_01
ORD IDord-62bc019b4b604012abbdb6abbcb6f7a7
Source noteuspto-grants-1983_01