Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Oxygen | HCID 977 | — |
| Reactant | Dimethyl Sulfide | HCID 1068 | — |
| Reactant | Dichloromethane | HCID 6344 | — |
| Reactant | HCID 54079479 | HCID 54079479 | — |
| Solvent | Methanol | HCID 887 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | HCID 23225813 | HCID 23225813 | — |
Reaction Steps
Combine N-t-butoxycarbonyl-N-allyl-2,2-bis-phenyl-ethylamine (0.23 g, 0.68 mmol) and dichloromethane (10 mL) and methanol (0.5 mL). Cool the -78° C. Pass ozonized oxygen through the solution until a persistent light blue color is obtained. Pass nitrogen through the solution until the blue color dissipates. Add dimethyl sulfide (2.0 mL). Allow the reaction mixture to warm to ambient temperature and stir for 5.5 hours. Concentrate in vacuo to obtain a residue. Dilute the residue with ethyl acetate and extract with water. Separate the layers, dry the organic layer over MgSO4, filter, and evaporate in vacuo to give the title compound.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05840726 |
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| Source dataset | uspto-grants-1998_11 |
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| ORD ID | ord-c8dd62c9858744dfb8a06f53b0a2a39a |
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| Source note | uspto-grants-1998_11 |
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