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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 266101Generated: November 1, 2026

Dimethyl Sulfoxide → HCID 18930351, compound

https://huagongshe.com/reaction/266101

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 (2.43 g, 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 numberUS05650416
Source datasetuspto-grants-1997_07
ORD IDord-5d33c0db259844288ccb333e5b24ba5a
Source noteuspto-grants-1997_07