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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 881Generated: October 23, 2026

Dimethyl Sulfoxide → HCID 178418459, compound

https://huagongshe.com/en/reaction/881

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDimethyl SulfoxideHCID 679—
ReactantTriethylamineHCID 8471—
ReactantOxalyl chlorideHCID 65578—
ReactantHCID 178418307HCID 178418307—
SolventDichloromethaneHCID 6344—
ProductHCID 178418459HCID 178418459—

Reaction Steps

To a -78° C. solution of oxalyl chloride (105 μL, 1.2 mmol) in 1.0 mL of methylene chloride was added dimethylsulfoxide (170 μL, 2.4 mmol). The resulting solution was stirred for 5 min and then 170 mg (0.6 mmol) of the alcohol 135 was added in 1.0 mL of methylene chloride. The reaction mixture was stirred at -78° C. for 45 min at which time 500 μL (3.6 mmol) of triethylamine was added and the solution was allowed to warm to ambient temperature. The reaction was quenched with 1.0N HCl and the aqueous layer was extracted with three portions of methylene chloride. The combined organic extracts were dried over MgSO4 and evaporated to dryness to give the crude aldehyde 136 which was used directly in the next reaction. 1H NMR consistent with structure.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05723459
Source datasetuspto-grants-1998_03
ORD IDord-2a5760aaa3d049789dc0038907f707bb
Source noteuspto-grants-1998_03