Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Water | HCID 962 | — |
| Reactant | Dichloromethane | HCID 6344 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | Trimethylsulfonium methyl sulfate | HCID 2760871 | — |
| Reactant | HCID 67946348 | HCID 67946348 | — |
| Product | HCID 54036889 | HCID 54036889 | 83% |
Reaction Steps
54 g of trimethylsulfonium methylsulfate and 120 ml of sodium hydroxide solution (50% strength by weight) are added to a solution of 84 g of 4-chlorophenyl β-methyl-2-chlorophenylstyryl ketone in 300 ml of methylene chloride. The reaction mixture is stirred for 12-15 hours at room temperature (20° C.), after which 300 ml of water are added to the solution and the organic phase is separated off. The organic phase isolated is washed twice with water, dried over sodium sulfate and evaporated down, 73 g (83%) of 2-(4-chlorophenyl)-2-(1-methyl-2-[2-chlorophenyl]-ethenyl)-oxirane being obtained.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05017595 |
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| Source dataset | uspto-grants-1991_05 |
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| ORD ID | ord-8d680d9554cb4362be81b06df88d5f95 |
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| Source note | uspto-grants-1991_05 |
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