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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2107774Generated: October 30, 2026

Dimethyl Sulfoxide → HCID 54249399, compound

https://huagongshe.com/reaction/2107774

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDimethyl SulfoxideHCID 679—
ReactantTriethylamineHCID 8471—
ReactantOxalyl chlorideHCID 65578—
ReactantHCID 19349402HCID 19349402—
SolventWaterHCID 962—
SolventDichloromethaneHCID 6344—
ProductHCID 54249399HCID 54249399—

Reaction Steps

A solution of oxalyl chloride (0.12 ml) in dichloromethane (2 ml) was stirred and cooled to 70° while dimethyl sulphoxide (0.12 ml) was added dropwise. The solution was stirred for 2 minutes, then 2-[3-(1-hydroxyethyl)-5-(1H-1,2,4-triazol-1-ylmethyl)phenyl]-2-methylpropiononitrile, (0.18 g), was added, and the temperature was kept at -70° for 10 minutes. Triethylamine (0.2 ml) was added, and the mixture was allowed to warm to room temperature. Water (15 ml) was added, and the mixture was extracted three times with dichloromethane. The extracts were combined, dried and evaporated to dryness, and the residue was purified by flash column chromatography, eluting with methanol:chloroform (1:99 by volume) to give 2-[3 acetyl-5-(1H-1,2,4-triazol-1 ylmethyl)phenyl]-2-methylpropiononitrile. Nmr in deuteriochloroform; δ 8.2(1H,s), 8.02(2H,m), 7.8(1H,m), 7.64(1H,m), 5.45(2H,s), 2.6 (3H,s), 1.75(6H,s).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04935437
Source datasetuspto-grants-1990_06
ORD IDord-ea4ab7f31ff84a55a66b2f3514d2b4d9
Source noteuspto-grants-1990_06