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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1759082Generated: October 30, 2026

Hydrochloric Acid → HCID 13469489, compound

https://huagongshe.com/reaction/1759082

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantWaterHCID 962—
ReactantSodium borohydrideHCID 4311764—
ReactantHCID 86736422HCID 86736422—
SolventEthanolHCID 702—
ProductHCID 13469489HCID 13469489—

Reaction Steps

To a suspended solution of benzyl 2-methyl-4-(2-nitrophenyl)-5-ethoxycarbonyl-6-formyl-1,4-dihydropyridine-3-carboxylate (1.2 g) in ethanol (20 ml) was added sodium borohydride (60.6 mg) under ice-cooling and stirred, and further stirred for an hour at 0° C. and another an hour at 3° C. The reaction mixture was added with water and the resultant mixture was adjusted to pH 6 to 7 with 2 N hydrochloric acid, and the solvent was distilled off. The residue was extracted with ethyl acetate and washed with water and dried. After removal of the solvent, the resultant oil (1.3 g) was purified by column chromatography on silica gel with an eluent (a mixture of ten parts of benzene and one part of ethyl acetate by volume) to give an oil which was immediately crystallized. The resultant crystals were recrystallized from a mixture of diethyl ether and n-hexane and dissolved in benzene. The benzene solution was subjected to azeotropic process five times to give pure crystals of benzyl 2-methyl-4-(2-nitrophenyl)-5-ethoxycarbonyl-6-hydroxymethyl-1,4-dihydropyridine-3-carboxylate, m.p. 51° to 57° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04338322
Source datasetuspto-grants-1982_07
ORD IDord-a6eb316b9b1e4255ba1669885fc06030
Source noteuspto-grants-1982_07