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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 458731Generated: October 30, 2026

Acetaldehyde → HCID 86597301, compound

https://huagongshe.com/reaction/458731

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetaldehydeHCID 177—
ReactantSodium cyanoborohydrideHCID 5003444—
ReactantHCID 69766274HCID 69766274—
SolventMethanolHCID 887—
SolventChloroformHCID 6212—
ProductHCID 86597301HCID 86597301—

Reaction Steps

To a solution of 25 mg of piperidin-4-yl (2R)-((1R)-3,3-difluorocyclopentyl)-2-hydroxy-2-(4-chlorophenyl)ethanoate in 1 ml of methanol, 50 mg of acetaldehyde and 10 mg of sodium cyanoborohydride were added at room temperature, followed by two hours' stirring at the same temperature. The reaction liquid was diluted with chloroform, washed successively with saturated sodium hydrogencarbonate solution and with saturated brine, and dried over anhydrous sodium sulfate. Distilling the solvent off under reduced pressure, the residue was purified on preparative thin layer chromatography (Kieselgel™60F254, Art5744 (Merck), chloroform/methanol=10/1) to provide the title compound.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07192969B2
Source datasetuspto-grants-2007_03
ORD IDord-396a9a494f5e4ac1b63da64972785bc8
Source noteuspto-grants-2007_03