HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1379960Generated: October 25, 2026
Oxygen → (S)-N-benzyl-N-methyl-2-[N-(t-butoxycarbonyl)-2-oxo-ethylamino]-3-phenyl-propionamide
https://huagongshe.com/reaction/1379960
Participants
| Role | Name | HCID | Charge |
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| Reactant | Oxygen | HCID 977 | — |
| Reactant | Pyridine | HCID 1049 | — |
| Reactant | Dimethyl Sulfide | HCID 1068 | — |
| Reactant | (S)-N-Benzyl-N-methyl-2-[N-(t-butoxycarbonyl)-allylamino]-3-phenyl-propionamide | HCID 54096526 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Solvent | Dichloromethane methanol | HCID 21226129 | — |
| Product | (S)-N-benzyl-N-methyl-2-[N-(t-butoxycarbonyl)-2-oxo-ethylamino]-3-phenyl-propionamide | HCID 53842533 | — |
Reaction Steps
Combine (S)-N-benzyl-N-methyl-2-[N'-(t-butoxycarbonyl)-allylamino]-3-phenyl-propionamide (10.04 g, 24.5 mmol), and pyridine (0.13 ml) in dichloromethane/methanol (300 mL/30 mL). Cool to -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 (55 mL). Allow the reaction mixture to warm to ambient temperature and stir for 16 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. Chromatograph on silica gel eluting with 10% ethyl acetate/hexane to give the title compound: TLC Rf =0.53 (silica gel, 10% ethyl acetate/hexane).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05672602 |
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| Source dataset | uspto-grants-1997_09 |
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| ORD ID | ord-270ec43201344f038523f49e1d8b2e67 |
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| Source note | uspto-grants-1997_09 |
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