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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 638003Generated: October 30, 2026

Acetone → HCID 20254912, compound

https://huagongshe.com/reaction/638003

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetoneHCID 180—
ReactantPrideperoneHCID 3050428—
ReactantSodium borohydrideHCID 4311764—
SolventEthanolHCID 702—
ProductHCID 20254912HCID 20254912—

Reaction Steps

0.38 g (0.01 mol) of sodium borohydride are added, while stirring, to a suspension of 4.1 g (0.01 mol) of 5-cyano-N-[2-[4-(p-fluorobenzoyl)-piperidinyl]ethyl]-2-methoxybenzamide in 50 ml of ethanol and the whole is stirred for 1 hour at room temperature. There is added to the resulting clear solution 1 ml of acetone and the whole is then concentrated in a water-jet vacuum. The residue is taken up in methylene chloride and water, the layers are separated in a separating funnel and, after being dried over magnesium sulphate, the organic phase is concentrated by evaporation. 5-Cyano-N-[2-[4-[(4-fluorophenyl)hydroxymethylene]-piperidinyl]-ethyl]-2-methoxybenzamide of melting point 135°-137° is obtained as residue.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04559349
Source datasetuspto-grants-1985_12
ORD IDord-4951b98718c7408589b4833f8edfb304
Source noteuspto-grants-1985_12