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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1873594Generated: November 1, 2026

Dimethyl Sulfoxide → HCID 178455320, compound

https://huagongshe.com/reaction/1873594

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDimethyl SulfoxideHCID 679—
ReactantTriethylamineHCID 8471—
ReactantOxalyl chlorideHCID 65578—
ReactantSodium BicarbonateHCID 516892—
ReactantHCID 178455321HCID 178455321—
SolventDichloromethaneHCID 6344—
ProductHCID 178455320HCID 178455320—

Reaction Conditions

Temperature-78 °C

Reaction Steps

16.4 g (129.47 mmol) oxalyl chloride are dissolved in 600 ml of dichloromethane and cooled to −78° C. 20.2 g (258.95 mmol) of dimethyl sulfoxide are then slowly added dropwise. The mixture is stirred for 5 min. After addition of a solution of 21.1 g (86.32 mmol) of the compound from Example 53A in 200 ml of dichloromethane the mixture is stirred at −78° C. for 1 h. 60 ml (431.58 mmol) of triethylamine are then slowly added dropwise. Over a period of one hour, the reaction mixture is then warmed to RT, and 500 ml of saturated aqueous sodium bicarbonate solution are then added. The phases are separated, the organic phase is dried over sodium sulfate and the solvent is removed on a rotary evaporator. The residue is purified chromatographically on silica gel 60 (mobile phase: gradient petroleum ether→petroleum ether/ethyl acetate 9:1).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08304412B2
Source datasetuspto-grants-2012_11
ORD IDord-1c4f3cd8115940508540c4a986214f97
Source noteuspto-grants-2012_11