Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 334261Generated: October 24, 2026

1-Phenylpiperazine → 1-(Biphenyl-2-ylmethyl)-4-phenylpiperazine

https://huagongshe.com/en/reaction/334261

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-PhenylpiperazineHCID 7096—
Reactant(1,1'-Biphenyl)-2-carboxaldehydeHCID 121052—
ReactantSodium triacetoxyborohydrideHCID 5049666—
SolventMethanolHCID 887—
SolventDichloromethaneHCID 6344—
SolventSodium BicarbonateHCID 516892—
Product1-(Biphenyl-2-ylmethyl)-4-phenylpiperazineHCID 7160252318.3%

Reaction Steps

1-Phenylpiperazine (266 mg, 1.64 mmol) was dissolved in methanol (7 mL) in a reaction vessel and, after adding biphenyl-2-carbaldehyde (150 mg, 0.82 mmol), the mixture was stirred at room temperature for 2 hours. 2 hours later, NaBH(OAc)3 (529 mg, 2.46 mmol) was added and the mixture was further stirred for 8 hours. After the reaction was completed, the reaction solution was diluted with dichloromethane and saturated NaHCO3 solution was added. After extraction, organic layer was dried with anhydrous MgSO4 and then filtered. The filtrate was concentrated and the concentrate was purified by column chromatography (hexane:diethyl ether=8:1) to obtain 50 mg of the target compound (0.15 mmol, 18.3%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08883796B2
Source datasetuspto-grants-2014_11
ORD IDord-3c743b5c80814404a61aa5b078ea4c0d
Source noteuspto-grants-2014_11