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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 485386Generated: October 27, 2026

Ethanol → HCID 178470502, compound

https://huagongshe.com/reaction/485386

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthanolHCID 702—
ReactantSodium borohydrideHCID 4311764—
Reactant4-[3-(1-Piperidinylmethyl)phenoxy]butanalHCID 21297547—
ReactantHCID 178499187HCID 178499187—
ProductHCID 178470502HCID 178470502—

Reaction Steps

Methyl 5-amino-1H-1,2,4-triazole-3-carboxylate (0.568 g) and 4-[3-(1-piperidinylmethyl)phenoxy]butanal in ethanol (40 ml) were heated at reflux for 2 h. The cooled reaction mixture was treated with sodium borohydride (0.4 g) and stirred at room temperature for 15 h. The solvent was evaporated and the residue was dissolved in 2N hydrochloric acid which was washed with ethyl acetate, basified with sodium carbonate and extracted with ethyl acetate. The combined organic extracts were evaporated to yield the title compound as a white solid which was recrystallised from a mixture of ethyl acetate and ethanol (1:1) (0.5 g) m.p. 170°-1° dec.; tlc System B, Rf 0.8.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04536508
Source datasetuspto-grants-1985_08
ORD IDord-32393270926f4dd58ed3dd761f6622d0
Source noteuspto-grants-1985_08