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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1649623Generated: November 2, 2026

Trimethylsulfonium iodide → 2-tert-Butyl-2-(3-phenoxypropyl)oxirane

https://huagongshe.com/reaction/1649623

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTrimethylsulfonium iodideHCID 75127—
ReactantHCID 14076005HCID 14076005—
SolventTetrahydrofuranHCID 8028—
Product2-tert-Butyl-2-(3-phenoxypropyl)oxiraneHCID 1407600881.2%

Reaction Steps

9 g (41 mMol) of 2,2-dimethyl-6-phenoxy-hexan-3-one are added dropwise to a mixture of 5.5 g (49 mMol) of potassium tert.-butylate in 40 ml of tetrahydrofuran at room temperature, with stirring, whereupon a clear yellowish solution forms. 12.5 g (61.5 mMol) of trimethylsulphonium iodide are then added and the mixture is stirred at 20° to 25° C. for 12 hours. Thereafter, the reaction mixture is filtered and the filtrate is concentrated under reduced pressure. The residue which remains is taken up in methylene chloride and the resulting solution is washed three times with water. After the organic phase has been dried, the solvent is stripped off. 7.8 g (81% of theory) of 2-(1,1-dimethyl-ethyl)-2-(3-phenoxypropyl)-oxirane are obtained in this manner in the form of a liquid of refractive index nD20 =1.503. ##STR13##

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04921529
Source datasetuspto-grants-1990_05
ORD IDord-52414ab9ff7e44d991e53980e3f41227
Source noteuspto-grants-1990_05