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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1450439Generated: October 29, 2026

Dimethyl Sulfoxide → HCID 18930351, compound

https://huagongshe.com/reaction/1450439

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDimethyl SulfoxideHCID 679—
ReactantTriethylamineHCID 8471—
ReactantOxalyl chlorideHCID 65578—
ReactantHCID 18930330HCID 18930330—
SolventDichloromethaneHCID 6344—
ProductHCID 18930351HCID 18930351—

Reaction Conditions

Temperature-78 °C

Reaction Steps

Dissolve oxalyl chloride (1.23 g, 9.67 mmol) in methylene chloride (100 mL), place under an argon atmosphere and cool to -78° C. Add dimethylsulfoxide (1.43 mL) and stir for 15 minutes. Add, by dropwise addition, a solution of α-[1-(2-phenylethyl)-4-piperidinyl]-2-thiophenemethanol 8.06 mmol) in methylene chloride (100 mL). Stir at -78° C. for 30 minutes, then add triethylamine (6.07 mL). Stir at -78° C. for 30 minutes, remove the ice bath and allow to warm to room temperature. Evaporate the solvent in vacuo and partition between methylene chloride and water. Separate the organic phase and extract the aqueous phase with methylene chloride. Combine the organic phases, wash with water and dry (MgSO4). Evaporate the solvent in vacuo and recrystallize (isopropanol) to give the title compound as a white crystalline solid; mp 77°-79° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05602147
Source datasetuspto-grants-1997_02
ORD IDord-7014446f1d274dc39ffb20b712c1dcba
Source noteuspto-grants-1997_02