Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1665978Generated: October 31, 2026

Dimethyl Sulfoxide → HCID 57508940, compound

https://huagongshe.com/reaction/1665978

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDimethyl SulfoxideHCID 679—
ReactantTriethylamineHCID 8471—
ReactantOxalyl chlorideHCID 65578—
ReactantHCID 57508939HCID 57508939—
SolventDichloromethaneHCID 6344—
ProductHCID 57508940HCID 5750894044.2%

Reaction Conditions

Temperature-40 °C

Reaction Steps

To a cold solution (−70° C.) of oxalyl chloride (169 mg, 1.34 mmol) and DMSO (209 mg, 2.67 mmol) in DCM (4 mL) a solution of {4-[5-(3-ethyl-5,5-dimethyl-4,5,6,7-tetrahydro-benzo[c]thiophen-1-yl)-[1,2,4]oxadiazol-3-yl]phenyl}-methanol (410 mg, 1.11 mmol) in DCM (5 mL) is added. The mixture is warmed to −40° C. within 30 min and then triethylamine (394 mg, 3.89 mmol) is added. Stirring is continued at −40° C. for 1 h, then at rt. The reaction is quenched by adding water and the mixture is extracted with diethyl ether. The organic extract is dried over MgSO4, filtered and the solvent of the filtrate is evaporated. The crude product is purified by chromatography on prep. TLC plates with heptane:EA 3:1 to give 4-[5-(3-ethyl-5,5-dimethyl-4,5,6,7-tetrahydro-benzo[c]thiophen-1-yl)-[1,2,4]oxadiazol-3-yl]-benzaldehyde (180 mg) as a white solid; LC-MS: tR=1.24 min, [M+1]+=367.24.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08039644B2
Source datasetuspto-grants-2011_10
ORD IDord-f13abe2a906a456ab4893905c1d22f23
Source noteuspto-grants-2011_10