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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2165188Generated: November 2, 2026

Dimethyl Sulfoxide → HCID 14537110, compound

https://huagongshe.com/reaction/2165188

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDimethyl SulfoxideHCID 679—
ReactantTriethylamineHCID 8471—
ReactantOxalyl chlorideHCID 65578—
ReactantHCID 14537109HCID 14537109—
SolventDichloromethaneHCID 6344—
ProductHCID 14537110HCID 1453711095.3%

Reaction Steps

An oven-dried 25 ml 2-necked (14/20) round bottom flask, equipped with magnetic stirring bar nitrogen inlet and serum cap, is charged with a solution of oxalyl chloride (61 μl) in 2 ml methylene chloride. This solution is placed under a nitrogen atmosphere and cooled to -60° C. to -50° C. Dimethylsulfoxide (99 μl) is added (neat) dropwise to give a colorless solution. After 2.3 min a solution of 3-[4-methoxy-1-[(tetrahydro-2H-pyran-2-yl)oxy]-2-naphthalenyl]-1-propanol (0.19 g) in 1 ml methylene chloride is added dropwise. The resulting mixture is stirred at -60° C. to -50° C. for 15 min and then treated with triethylamine (0.44 ml). This gives rise to a yellow colored milky suspension. The cooling bath is removed and the stirred mixture is allowed to warm to room temperature at which time the mixture is diluted with water and extracted with ether. The organic phase is washed three times with water (after adjusting the pH to 7 with 10% aqueous sodium bisulfate), dried with magnesium sulfate, filtered and concentrated to give 0.18 g of the crude title compound as an orange colored oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04939169
Source datasetuspto-grants-1990_07
ORD IDord-6e60cef592bf4aea8743620866d6b766
Source noteuspto-grants-1990_07