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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 865936Generated: October 31, 2026

3-Acetylbenzonitrile → HCID 10521779, compound

https://huagongshe.com/reaction/865936

Reaction equation

Participants

RoleNameHCIDCharge
Reactant3-AcetylbenzonitrileHCID 80222—
ReactantSodium borohydrideHCID 4311764—
Reactant1-[2-(Propan-2-yloxy)phenyl]piperazineHCID 10944016—
CatalystTitanium isopropoxideHCID 11026—
SolventMethanolHCID 887—
ProductHCID 10521779HCID 1052177913.5%

Reaction Steps

A mixture of 1-[2-(methylethoxy)phenyl]piperazine (IPP, 7.28 g, 0.033 mol), 3-acetylbenzonitrile (4.80 g, 0.033 mol), and titanium isopropoxide (11.74 g, 0.041 mol) was stirred at room temperature for 2 h, heated to 80° C. for several minutes, and then cooled to room temperature. Methanol (150 mL) was added and the mixture was heated to dissolve most of the solids. After cooling to room temperature, sodium borohydride (2.27 g, 0.060 mol) was added in portions and the mixture was stirred overnight at room temperature. The reaction mixture was concentrated on a rotary evaporator and the residue was partitioned between 3N NaOH/CH2Cl2. The organic layer was separated, dried (K2CO3), filtered, and evaporated to an oily residue which was passed through flash grade silica using 4:1 hexane:EtOAc as eluant to give 3-[1-[4-[2-(1-methylethoxy)phenyl]-1-piperazinyl]ethyl]benzonitrile as an oil (1.55 g, 13.5%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05569659
Source datasetuspto-grants-1996_10
ORD IDord-377eefd82ac446c19229c87403c1f00a
Source noteuspto-grants-1996_10