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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1589981Generated: November 3, 2026

Dimethyl Sulfoxide → HCID 14834351, compound

https://huagongshe.com/reaction/1589981

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDimethyl SulfoxideHCID 679—
ReactantTriethylamineHCID 8471—
ReactantOxalyl chlorideHCID 65578—
ReactantHCID 10997486HCID 10997486—
SolventWaterHCID 962—
SolventDichloromethaneHCID 6344—
ProductHCID 14834351HCID 1483435198.5%

Reaction Conditions

Temperature25 °C

Reaction Steps

A solution of 117.0 g (1.5 moles) of dimethylsulfoxide in 300 ml of dichloromethane was added dropwise to a solution of 83.8 g (0.66 mole) of oxalyl chloride in 750 ml of dichloromethane at -60° C. The reaction mixture was stirred for 15 minutes at this temperature, after which 102.6 g (0.6 mole) of 3-tert-butyl-5-hydroxymethyl-5-methylisoxazoline were added and stirring was continued for a further 15 minutes. After the dropwise addition of 303.6 g (3.0 moles) of triethylamine, the mixture was stirred for a further 10 minutes and was heated to 25° C. and 1.8 l of water were added. After 10 minutes, the organic phase was seperated off, the aqueous phase was extracted with twice 600 ml of dichloromethane and the combined organic phases were washed with three times 450 ml of a 1N hydrochloric acid and once with 450 ml of a saturated sodium carbonate solution, dried and evaporated down. 100 g of a yellow liquid were obtained, this liquid being subjected to fractional distillation under 0.2 mbar.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05201935
Source datasetuspto-grants-1993_04
ORD IDord-a9ce1ce92803481f9fd75b09a8bdda6d
Source noteuspto-grants-1993_04