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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1754184Generated: November 3, 2026

3-Hydroxybenzaldehyde → 4-(3-hydroxybenzyl)-N-phenylpiperazine-1-carboxamide

https://huagongshe.com/reaction/1754184

Reaction equation

Participants

RoleNameHCIDCharge
Reactant3-HydroxybenzaldehydeHCID 101—
ReactantHydrochloric AcidHCID 313—
ReactantSodium HydroxideHCID 14798—
ReactantSodium triacetoxyborohydrideHCID 5049666—
ReactantN-phenylpiperazine-1-carboxamideHCID 7015289—
SolventAcetic AcidHCID 176—
SolventDichloromethaneHCID 6344—
Product4-(3-hydroxybenzyl)-N-phenylpiperazine-1-carboxamideHCID 5110622982.4%

Reaction Steps

To a solution of piperazine-1-carboxylic acid phenylamide (2.0 g) and 3-hydroxybenzaldehyde (3.0 g) in DCM (200 mL) was added acetic acid (1.1 mL) followed by portion-wise addition of NaB(OAc)3H (6.0 g). The reaction mixture was stirred overnight. A solution of 10% aq. NaOH (30 mL) was added until the pH of the aqueous phase was 11. A solution of 1 N HCl was then added until the pH of the aqueous phase was 6-7. The aqueous phase was extracted with DCM (200 mL). The combined organic layers were dried (MgSO4) and concentrated. Chromatography of the residue gave the title compound as a white solid (2.5 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09169224B2
Source datasetuspto-grants-2015_10
ORD IDord-a901b0382c4741869e97872e60816c60
Source noteuspto-grants-2015_10