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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1368206Generated: November 2, 2026

Dimethyl Sulfoxide → HCID 22264737, compound

https://huagongshe.com/reaction/1368206

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDimethyl SulfoxideHCID 679—
ReactantTriethylamineHCID 8471—
ReactantOxalyl chlorideHCID 65578—
ReactantHCID 11463910HCID 11463910—
SolventDichloromethaneHCID 6344—
ProductHCID 22264737HCID 2226473793.3%

Reaction Conditions

Temperature-50 °C

Reaction Steps

To a solution of oxalyl chloride (0.62 g, 5 mmol) in CH2Cl2 (20 mL) at −50° C. was added DMSO (0.85 g, 11 mmol, in solution of 5 mL of CH2Cl2) over 2 minutes. 4-(4-fluorobenzyl)-1-((4-chlorophenoxy)methyl)carbonyl-3-(2-hydroxyethyl)piperazine (1.85 g, 4.5 mmol, in solution of 5 mL of CH2Cl2) was added. The resulting mixture was stirred at −50° C. for 15 minutes, then triethylamine (2.3 g, 22 mmol) was added. After 5 minutes at −50° C., the mixture was gradually warmed to ambient temperature. At that time the mixture was diluted with CH2Cl2 and washed with water, then brine. The organic layer was then dried over MgSO4 and concentrated in vacuo to afford 1.7 g of 4-(4-fluorobenzyl)-1-((4-chlorophenoxy)methyl)carbonyl-3-((formyl)methyl)piperazine as a yellow oil; NMR (CDCl3) 9.8 (d, 1) 7.3 (m, 4), 7.0 (m, 4), 4.6 (m, 3), 3.8-3.2 (m, 7), 2.7-2.2 (m, 4) ppm.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06573266B1
Source datasetuspto-grants-2003_06
ORD IDord-8cf717eed1f94bbba574a00caf98f4e1
Source noteuspto-grants-2003_06