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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1164613Generated: October 29, 2026

Hexane → Diethyl 2-methyl-4-(2-thienyl)-6-hydroxymethyl-1,4-dihydropyridine-3,5-dicarboxylate

https://huagongshe.com/reaction/1164613

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHexaneHCID 8058—
ReactantSodium borohydrideHCID 4311764—
ReactantDiethyl 2-methyl-4-(2-thienyl)-6-formyl-1,4-dihydropyridine-3,5-dicarboxylateHCID 11245008—
SolventEthanolHCID 702—
SolventEthyl AcetateHCID 8857—
ProductDiethyl 2-methyl-4-(2-thienyl)-6-hydroxymethyl-1,4-dihydropyridine-3,5-dicarboxylateHCID 1346947290.6%

Reaction Steps

To a solution of diethyl 2-methyl-4-(2-thienyl)-6-formyl-1,4-dihydropyridine-3,5-dicarboxylate (940.68 mg) in 99% ethanol (30 ml) was gradually added sodium borohydride (113.5 mg) under stirring and this was further stirred at room temperature for 2 hours. After removal of ethanol, the residue was extracted with ethyl acetate and the extract was washed twice with water and then dried. The solvent was removed from the extract to give a pale yellow oil. The oil was pulverized with n-hexane. The powder was dissolved in ethyl acetate. After collecting by filtration of the insoluble product, to the filtrate was added n-hexane and the mixture was allowed to stand in refrigerator. The appearring crystals were collected by filtration to give pale yellow granules (857.2 mg) of diethyl 2-methyl-4-(2-thienyl)-6-hydroxymethyl-1,4-dihydropyridine-3,5-dicarboxylate, m.p. 125° to 126° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04370334
Source datasetuspto-grants-1983_01
ORD IDord-81f6713b422646d4ba74b587b836c3c8
Source noteuspto-grants-1983_01