Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 563145Generated: October 29, 2026

4-Butoxybenzaldehyde → HCID 59808329, compound

https://huagongshe.com/reaction/563145

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-ButoxybenzaldehydeHCID 79813—
ReactantDiisopropylethylamineHCID 81531—
ReactantSodium borohydrideHCID 4311764—
ReactantHCID 67005485HCID 67005485—
SolventMethanolHCID 887—
SolventWaterHCID 962—
ProductHCID 59808329HCID 5980832967.2%

Reaction Steps

2-Amino-1-(4-benzyl-piperazin-1-yl)-(S)-3-phenyl-propan-1-one hydrochloride (500 mg, 1.26 mmol) were dissolved in MeOH (5 mL), DIPEA (359 mg, 2.77 mmol) and 4-n-butoxybenzaldehyde (226 mg, 1.26 mmol) was added and the mixture was heated to reflux for 2 h, cooled again to rt followed by slow addition of sodium borohydride (48 mg, 1.26 mmol) in portions. Stirring was continued for 15 min. Water (1 mL) was added and the solvents were removed under reduced pressure. The residue was taken up in diethylether (5 mL), washed with 10% aq. citric acid (5 mL) and water (5 mL), dried over magnesium sulfate, filtered and concentrated in vacuo to give 411 mg (67%) of 1-(4-benzyl-piperazin-1-yl)-2-(4-butoxy-benzylamino)-(S)-3-phenyl-propan-1-one. LC-MS: tR=0.74 min; [M+H]+=486.43.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08067419B2
Source datasetuspto-grants-2011_11
ORD IDord-edc50b27b88c4e86aea8c5d833b9b7b9
Source noteuspto-grants-2011_11