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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1246931Generated: October 31, 2026

Dimethyl Sulfoxide → HCID 21904386, compound

https://huagongshe.com/reaction/1246931

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDimethyl SulfoxideHCID 679—
ReactantOxalyl chlorideHCID 65578—
ReactantSodium BicarbonateHCID 516892—
ReactantHCID 21904380HCID 21904380—
SolventMethanolHCID 887—
SolventDichloromethaneHCID 6344—
SolventTriethylamineHCID 8471—
ProductHCID 21904386HCID 21904386—

Reaction Steps

To a solution of oxalyl chloride (0.22 ml, 2.54 mmol) in CH2Cl2 (2 ml) at −55 ° C. was added a solution of DMSO (0.30 ml, 4.24 mmol) in CH2Cl2 (1 ml). The mixture was stirred for 2 min. Then, a solution of 173 (230 mg, 1.06 mmol) in CH2Cl2 (1 ml) was added dropwise. After stirring for 15 min at −55° C., Et3N (1.4 ml) was added slowly. The mixture was stirred for 5 min and then warmed to room temperature. Aqueous NaHCO3 (5 ml) was added. The two layers were separated; and the aqueous layer was extracted with CH2Cl2 (2×5 ml). The combined organics were dried (Na2SO4), filtered and evaporated to give the crude product. Chromatography (1% MeOH in CH2Cl2) gave 174 as a light red liquid. 1 H-NMR (300 MHz, CDCl3) (partial) δ 9.42 (s, 1H), 7.30 (m, 5H); LRMS (calculated for C14H17NO) 215. found 215.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07129228B2
Source datasetuspto-grants-2006_10
ORD IDord-ab3e77d66d4f494f9eca7e41b025d17d
Source noteuspto-grants-2006_10