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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1947076Generated: November 1, 2026

4-Chlorobenzaldehyde → HCID 11510335, compound

https://huagongshe.com/reaction/1947076

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-ChlorobenzaldehydeHCID 7726—
ReactantSodium AcetateHCID 517045—
ReactantSodium cyanoborohydrideHCID 5003444—
ReactantHCID 68513589HCID 68513589—
SolventMethanolHCID 887—
ProductHCID 11510335HCID 1151033556%

Reaction Steps

(4-Chloro-phenyl)-(3-hydroxy-4-piperazin-1-yl-pyrrolidin-1-yl)-methanone hydrochloride (100 mg, 0.290 mmol), NaCNBH3 (20 mg, 0.319 mmol), NaOAc (23.8 mg, 0.29 mmol), 4-chloro-benzaldehyde (42.8 mg, 0.30 mmol) were added to methanol (3 mL). The reaction mixture was stirred in room temperature for over night. The mixture was concentrated. K2CO3 and Ethyl acetate were added to the residue. The organic phase was washed with brine, dried over Na2SO4, and concentrated. The crude was purified by column chromatography to give 70 mg of desired product as an oil (56% yield).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08399455B2
Source datasetuspto-grants-2013_03
ORD IDord-a5fbdb98111749d6975e3e3878534d66
Source noteuspto-grants-2013_03