Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 743036Generated: October 30, 2026

1-Piperazinecarboxaldehyde → HCID 19421679, compound

https://huagongshe.com/reaction/743036

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-PiperazinecarboxaldehydeHCID 82191—
ReactantP,P-Diphenylphosphinic azideHCID 199401—
ReactantSodium BicarbonateHCID 516892—
ReactantHCID 12660800HCID 12660800—
SolventDichloromethaneHCID 6344—
SolventTriethylamineHCID 8471—
ProductHCID 19421679HCID 19421679—

Reaction Steps

3,41 ml of diphenylphosphoryl azide and 1.09 ml of 1-formylpiperazine were added to a 60 ml of a methylene chloride solution of 3.00 g of 3,3-bis(4-methoxyphenyl)acrylic acid and 2.94 ml of triethylamine. The reaction mixture was then stirred for2 hours at room temperature, after which it was poured into a saturated aqueous solution of sodium bicarbonate and extracted twice with methylene chloride. The combined extracts were washed with water, dried over anhydrous sodium sulfate and evaporated under reduced pressure. The residue was dissolved in 80 ml of methanol, and 40 ml of a 10% w/v aqueous solution of sodium hydroxide were added to the resulting solution. The reaction mixture was stirred for 18 hours at room temperature and then poured into water: it was then extracted twice with methylene chloride. The combined extracts were washed with water, dried over anhydrous sodium sulfate and evaporated under reduced pressure. The residue was purified by column chromatography through 80 g of silica gel eluted with mixtures of methylene chloride and methanol ranging from 19:1 to 4:1 by volume to give 3.00 g of 1-[3,3-bis(4-methoxyphenyl)acryloyl]piperazine as a powder.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05556852
Source datasetuspto-grants-1996_09
ORD IDord-e3b92833b9c2462b94a215b78ef46c8d
Source noteuspto-grants-1996_09