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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1807863Generated: October 30, 2026

Dimethyl Sulfoxide → HCID 178520959, compound

https://huagongshe.com/reaction/1807863

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDimethyl SulfoxideHCID 679—
ReactantTriethylamineHCID 8471—
ReactantOxalyl chlorideHCID 65578—
ReactantHCID 178525075HCID 178525075—
SolventWaterHCID 962—
SolventDichloromethaneHCID 6344—
ProductHCID 178520959HCID 17852095994.9%

Reaction Conditions

Temperature-78 °C

Reaction Steps

Under nitrogen air flow, to a solution of 0.73 mL of oxalyl chloride in 13 mL of dichloromethane was added dropwise a mixed liquid of 1.23 mL of dimethylsulfoxide and 14 mL of dichloromethane at −78° C. First, a solution of 1.70 g of the obtained benzyl trans-4-(hydroxymethyl)cyclohexane carboxylate in 20 mL of dichloromethane was added dropwise to the reaction mixture at −78° C. After stirring at −78° C. for 0.5 hours, triethylamine was added thereto at −78° C., followed by stirring at −65° C. for 2 hours. The reaction liquid was warmed to room temperature, dichloromethane and water were added thereto, and the aqueous layer was separated. The organic layer was washed with water, 1 M hydrochloric acid, a saturated aqueous sodium hydrogen carbonate solution, and saturated brine in this order, and dried over anhydrous sodium sulfate, and then the solvent was evaporated to obtain 1.60 g of benzyl trans-4-formylcyclohexanecarboxylate.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08357688B2
Source datasetuspto-grants-2013_01
ORD IDord-b6fd9e5db1114dbc9c96b05a2033c3e0
Source noteuspto-grants-2013_01