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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1806910Generated: October 29, 2026

Dimethyl Sulfoxide → HCID 12721744, compound

https://huagongshe.com/reaction/1806910

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDimethyl SulfoxideHCID 679—
ReactantTriethylamineHCID 8471—
ReactantOxalyl chlorideHCID 65578—
Reactant2-(1-Methylcyclohexyl)ethanolHCID 231930—
SolventWaterHCID 962—
SolventDichloromethaneHCID 6344—
ProductHCID 12721744HCID 1272174491.4%

Reaction Conditions

Temperature-78 °C

Reaction Steps

Step D To a solution of oxalyl chloride (2.18 g, 17.2 mmol) (Aldrich) in dichloromethane (12 mL) at −78° C. was added the solution of dimethyl sulfoxide (2.44 mL, 34.3 mmol) in dichloromethane (8 mL) dropwise. After 5 mins, the solution of 2-(1-methyl-cyclohexyl)-ethanol (2.2 g, 15.6 mmol) in dichloromethane (10 mL) was added dropwise. The reaction mixture was stirred at −78° C. for 15 min. Triethylamine (7.8 mL, 56 mmol) was added and the reaction mixture was slowly warmed up to room temperature and stirred at room temperature for 45 min. Then water was added. The organic layers were separated, and the aqueous layer was extracted with dichloromethane. The organic layers were combined, washed with 10% of HCl, saturated NaHCO3, brine, dried over MgSO4, and concentrated to give (1-methyl-cyclohexyl)-acetaldehyde as a light yellow oil (Yield: 2 g, 91%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08354444B2
Source datasetuspto-grants-2013_01
ORD IDord-d411062f52694ff8ad8780a592fdd392
Source noteuspto-grants-2013_01