Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 894687Generated: November 1, 2026

Acetic Acid → HCID 13469488, compound

https://huagongshe.com/reaction/894687

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AcidHCID 176—
ReactantSodium borohydrideHCID 4311764—
ReactantHCID 20574379HCID 20574379—
SolventEthanolHCID 702—
ProductHCID 13469488HCID 1346948849.3%

Reaction Steps

To a solution of 2-hydroxyethyl 2-methyl-4-(2-nitrophenyl)-5-ethoxycarbonyl-6-formyl-1,4-dihydropyridine-3-carboxylate (2.0 g) in ethanol (40 ml) was added bit-by-bit sodium borohydride (113.5 mg) at 5° C. under stirring. The mixture was further stirred at 5° C. for 30 minutes and acidified weakly with 50% acetic acid. After removal of the ethanol, to the residue was added water, and the mixture was made slightly alkaline with an aqueous solution of sodium bicarbonate, allowed to stand and then filtered, when it became clear. The precipitate (1.58 g) was collected by filtration and, recrystallized from a mixture of ethanol and diisopropyl ether to give yellowish-orange granules (0.99 g) of 2-hydroxyethyl 2-methyl-4-(2-nitrophenyl)-5-ethoxycarbonyl-6-hydroxymethyl-1,4-dihydropyridine-3-carboxylate, m.p. 167° to 169° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04284634
Source datasetuspto-grants-1981_08
ORD IDord-e12f2bb9850e458aa3aa162ba63a2a4a
Source noteuspto-grants-1981_08