Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1596554Generated: October 30, 2026

Dimethyl Sulfoxide → HCID 18466676, compound

https://huagongshe.com/reaction/1596554

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDimethyl SulfoxideHCID 679—
ReactantTriethylamineHCID 8471—
ReactantOxalyl chlorideHCID 65578—
ReactantHCID 18466815HCID 18466815—
SolventWaterHCID 962—
SolventDichloromethaneHCID 6344—
ProductHCID 18466676HCID 1846667649.8%

Reaction Conditions

Temperature-60 °C

Reaction Steps

A solution of 0.2 ml of dimethyl sulfoxide in 1 ml of methylene chloride was dropped into a solution of 0.124 ml of oxalyl chloride in 10 ml of methylene chloride cooled to −60° C., followed by the stirring for 5 minutes. A solution of 0.5 g of methyl 4-[(3,4,6,7,8,9-hexahydro-6,6,9,9-tetramethyl-1(2H)-phenazinon-2-yl)hydroxymethyl]benzoate in 10 ml of methylene chloride was dropped into the solution prepared above. The obtained mixture was stirred for 15 minutes, followed by the dropwise addition of 0.954 ml of triethylamine. The temperature of the reaction mixture was raised to room temperature. The resulting mixture was stirred for 30 minutes, followed by the addition of water. The obtained mixture was extracted with methylene chloride. The organic phase was washed with water and a saturated aqueous solution of common salt, dried over anhydrous magnesium. sulfate and concentrated in a vacuum. The residue was purified by silica gel chromatography (developer: 5% ethyl acetate/hexane) to give 0.248 g of the title compound as a pale-yellow oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06291508B1
Source datasetuspto-grants-2001_09
ORD IDord-ad80c42161914286ba8f98e3188d16d5
Source noteuspto-grants-2001_09