HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2072219Generated: October 31, 2026
4,4-Diphenyl-2-butanone → 2-(2,2-Diphenylethyl)-2-methyloxirane
https://huagongshe.com/reaction/2072219
Participants
| Role | Name | HCID | Charge |
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| Reactant | 4,4-Diphenyl-2-butanone | HCID 79421 | — |
| Reactant | Dimethylsulfoxonium methylide | HCID 6396768 | — |
| Product | 2-(2,2-Diphenylethyl)-2-methyloxirane | HCID 21411073 | — |
Reaction Steps
The 1,2-epoxy-4,4-diarylbutane starting materials can alternatively be prepared by reaction of dimethylsulfonium methylide or dimethyloxosulfonium methylide with an appropriate diarylalkyl aldehyde or a diarylalkyl ketone. For example, reaction of an aldehyde such as 3,3-diphenylpropanal with either dimethylsulfonium methylide or dimethyloxosulfonium methylide in approximately equimolar amounts provides 1,2-epoxy-4,4-diphenylbutane. Similarly, reaction of a diarylalkyl ketone such as methyl-(2,2-diphenylethyl) ketone with either dimethylsulfonium methylide or dimethyloxosulfonium methylide provides 1,2-epoxy-4,4-diphenyl-2-methylbutane. Such reactions typically are carried out in a solvent such as dimethyl sulfoxide or tetrahydrofuran, and normally at a reduced temperature of about 0° C. Dimethylsulfonium methylide is prepared by reaction of trimethylsulfonium iodide with methylsulfinylcarbanion, while demethyloxosulfonium methylide is prepared by reaction of trimethyloxosulfonium iodide with sodium hydride. Such reactions are more fully discussed by Corey et al., J. Am. Chem. Soc., 84, 867(1962) and J. Am. Chem. Soc., 84, 3782 (1962).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04049827 |
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| Source dataset | uspto-grants-1977_09 |
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| ORD ID | ord-dcd226a6072b4a9db0487d37e1ad0d51 |
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| Source note | uspto-grants-1977_09 |
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