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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2380964Generated: October 30, 2026

4-Cyanobenzaldehyde → HCID 67130691, compound

https://huagongshe.com/reaction/2380964

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-CyanobenzaldehydeHCID 66042—
ReactantSodium borohydrideHCID 4311764—
Reactant(4-Aminophenyl)(4-phenylpiperazin-1-yl)methanoneHCID 12932882—
SolventTetrahydrofuranHCID 8028—
ProductHCID 67130691HCID 67130691—

Reaction Conditions

Temperature50 °C

Reaction Steps

To a stirred solution of (4-amino-phenyl)-(4-phenyl-piperazin-1-yl)-methanone (0.5 g, 1.78 mmol) in tetrahydrofuran (10 mL) was added 4-cyanobenzaldehyde (0.4 g, 2.67 mmol) followed by sodium borohydride and the reaction was heated to 50° C. for 2 hours. On cooling, the reaction was quenched by the addition of water (10 mL) and the aqueous solution basified by the addition of ammonium chloride (˜pH 8). The aqueous mixture was extracted using dichloromethane (3×10 ml) and the organic extracts combined, dried over magnesium sulfate and concentrated in vacuo to afford the title compound as an off white solid (604 mg, 98% yield). HPLC retention time 7.17 min. Mass spectrum (ES+) m/z 397 (M+H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08258138B2
Source datasetuspto-grants-2012_09
ORD IDord-9606026e63184e11923a209257b8e1db
Source noteuspto-grants-2012_09