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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 131407Generated: October 27, 2026

Dimethyl Sulfoxide → (S)-(1,4-dibenzyl-piperazin-2-yl)-acetaldehyde

https://huagongshe.com/reaction/131407

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDimethyl SulfoxideHCID 679—
ReactantTriethylamineHCID 8471—
ReactantAmmonium ChlorideHCID 25517—
ReactantOxalyl chlorideHCID 65578—
Reactant(1,4-Dibenzyl-piperazin-2-yl)-ethanolHCID 21295699—
SolventDichloromethaneHCID 6344—
SolventEthyl AcetateHCID 8857—
Product(S)-(1,4-dibenzyl-piperazin-2-yl)-acetaldehydeHCID 59732114—

Reaction Conditions

Temperature-78 °C

Reaction Steps

Add anhydrous DMSO (3.57 mL, 50.25 mmol) in anhydrous dichloromethane (68.0 mL). Cool to −78° C. and stir. Add oxalyl chloride (2M in dichloromethane, 12.06 mL, 24.125 mmol) dropwise. Stir at −78° C. for 30 minutes. Add (1,4-dibenzyl-piperazin-2-yl)-ethanol (6.241 g, 20.1 mmol) in dichloromethane (12.0 mL) and stir. After 1 hour, add triethylamine (14.01 mL, 100.5 mmol) and stir for another 1 hour. Allow the reaction mixture gradually warm to ambient temperature. Add saturated ammonium chloride. (200 mL). Exact aqueous portion with ethyl acetate three times. Combine the organic solution, dry over sodium sulfate, filter, and concentrate under reduced pressure to give crude residue. Purify the residue by flash chromatography, eluting with 2M ammonia in methanol:dichloromethane (5:95) to give the title compound: mass spectrum (m/e):309.03 (M+1).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07384934B2
Source datasetuspto-grants-2008_06
ORD IDord-4a4d8c8437d7447c8ad4a28c3d1278f3
Source noteuspto-grants-2008_06