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
Participants
| Role | Name | HCID | Charge |
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| Reactant | Trimethylsulfonium iodide | HCID 75127 | — |
| Reactant | HCID 14076005 | HCID 14076005 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 2-tert-Butyl-2-(3-phenoxypropyl)oxirane | HCID 14076008 | 81.2% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04921529 |
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| Source dataset | uspto-grants-1990_05 |
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| ORD ID | ord-52414ab9ff7e44d991e53980e3f41227 |
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| Source note | uspto-grants-1990_05 |
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