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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1249395Generated: November 3, 2026

Dimethyl Sulfoxide → HCID 13532506, compound

https://huagongshe.com/reaction/1249395

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDimethyl SulfoxideHCID 679—
ReactantSodium hydrideHCID 24758—
ReactantSulfoxonium, trimethyl-, iodide (1:1)HCID 74498—
ReactantHCID 13532505HCID 13532505—
SolventWaterHCID 962—
ProductHCID 13532506HCID 13532506—

Reaction Conditions

Temperature60 °C

Reaction Steps

1.5 g (0.05 mol) of 80% pure sodium hydride are added in portions to a mixture of 11 g (0.05 mol) of trimethylsulphoxonium iodide and 60 ml of dimethylsulphoxide at 10° C., with stirring. The reaction mixture is stirred for 15 minutes, 17.7 g (0.05 mol) of 3-(4-chlorobenzyloxy)-(6-chloropyridin-2-yloxy)-3-methyl-2-butanone in a little dimethylsulphoxide are then added dropwise and the mixture is warmed at 60° C. for 1 hour. It is subsequently poured into water, under a nitrogen atmosphere, and extracted with methylene chloride. The organic phase is dried over sodium sulphate and concentrated. The crude 2-[2-(4-chlorobenzyloxy)-prop-2-yl]-2-(6-chloropyridin-2-yloxymethyl)-oxirane thus obtained is further reacted directly. ##STR13##

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04631288
Source datasetuspto-grants-1986_12
ORD IDord-f409a5f2a1cc4bafb2c88f5da30c4ee0
Source noteuspto-grants-1986_12