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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1986961Generated: November 2, 2026

Dimethyl Sulfoxide → HCID 86591120, compound

https://huagongshe.com/reaction/1986961

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDimethyl SulfoxideHCID 679—
ReactantTriethylamineHCID 8471—
ReactantOxalyl chlorideHCID 65578—
ReactantHCID 68994515HCID 68994515—
SolventDichloromethaneHCID 6344—
ProductHCID 86591120HCID 86591120—

Reaction Steps

A solution of oxalyl chloride (62 μl, 0.72 mmol) in anhydrous methylene chloride (10 ml) under N2 was cooled to −78° C. while stirring. Dimethy sulfoxide (104 μl, 1.44 mmol) was then added followed by a solution of {(1R,2R)-2-[4-(6-Trifluoromethyl-benzo[b]thiophen-3-yl)-piperazin-1-ylmethyl]-cyclopropyl}-methanol (0.135 g, .36 mmol) in anhydrous methylene chloride (10 ml). Stirring was continued at −78° for 35 minutes and then triethyl amine (1.0 ml, .7.3 mmol) was added. This solution was stirred for 4 hours and then removed from the cold bath, filtered, concentrated and chromatagraphed on silica gel with methylene chloride/methanol (95:5). The resultant pure aldehyde, (1R,2R)-2-[4-(6-Trifluoromethyl-benzo[b]thiophen-3-yl)-piperazin-1-ylmethyl]-cyclopropanecarbaldehyde was verified by NMR and LC/MS, yielding 0.102 g, 76%.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07550469B2
Source datasetuspto-grants-2009_06
ORD IDord-5053432a06e84a109caf025e03967898
Source noteuspto-grants-2009_06