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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1750727Generated: October 27, 2026

3,3-Diphenylacrolein → Ethyl 4-(4-(3,3-diphenylallyl)piperazin-1-yl)benzoate

https://huagongshe.com/reaction/1750727

Reaction equation

Participants

RoleNameHCIDCharge
Reactant3,3-DiphenylacroleinHCID 71027—
ReactantCyano-borohydrideHCID 498716—
ReactantEthyl 4-(piperazin-1-yl)benzoateHCID 2761178—
SolventMethanolHCID 887—
SolventDichloromethaneHCID 6344—
ProductEthyl 4-(4-(3,3-diphenylallyl)piperazin-1-yl)benzoateHCID 67144443—

Reaction Steps

A suspension of ethyl 4-piperazin-1-ylbenzoate (1.36 g) and 3,3-diphenylacrylaldehyde (1.56 g) in dichloromethane (10 mL) and methanol (10 mL) was treated with polymer-supported cyanoborohydride (2.47 mmol/g, 6 g), shaken at room temperature for 24 hours, and filtered. The resin was washed with 1:1 dichloromethane/methanol (10 mL×3) and the combined filtrates were concentrated. The concentrate was purified by silica gel chromatography eluting with a gradient from 10%-50% ethyl acetate/hexanes to provide the desired product.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09156856B2
Source datasetuspto-grants-2015_10
ORD IDord-cca96db529334ef887db242389c61f87
Source noteuspto-grants-2015_10