HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2242639Generated: October 30, 2026
Methyl morpholine oxide → 1-N-Cbz-3-pyrrolidinone
https://huagongshe.com/reaction/2242639
Participants
| Role | Name | HCID | Charge |
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| Reactant | Methyl morpholine oxide | HCID 82029 | — |
| Reactant | (R)-(-)-1-CBZ-3-pyrrolidinol | HCID 11183628 | — |
| Catalyst | HCID 178419074 | HCID 178419074 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 1-N-Cbz-3-pyrrolidinone | HCID 561203 | — |
Reaction Steps
A 12-L, 3 neck round bottom flask equipped with a mechanical stirrer, thermocouple, condenser, and nitrogen bubbler was charged with 351 g (1.61 mol) of benzyl (3R)-3-hydroxypyrrolidine-1-carboxylate (Intermediate 1, Step A), 6 L of dichloromethane, 500 g of powdered molecular sieves, and 400 g (3.41 mol) of N-methylmorpholine-N-oxide. The resultant suspension was stirred at ambient temperature and to this was added 12.9 g (0.0367 mol) of tetrapropylammonium perruthenate. The reaction temperature was kept at ≦30° C. with a cold water bath. The mixture was stirred at ambient temperature for 2 h. The mixture was poured onto a plug of 5 kg of silica gel and eluted with 10% ethyl acetate/dichloromethane to give the title compound as an orange oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07671073B2 |
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| Source dataset | uspto-grants-2010_03 |
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| ORD ID | ord-14d14710cb3043a1a195a20503192e5c |
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| Source note | uspto-grants-2010_03 |
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