HuagongsheHuagongshe Chemistry Print Report · For research reference only
Methyl morpholine oxide → tert-Butyl 4-formylpiperidine-1-carboxylate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Methyl morpholine oxide | HCID 82029 | — |
| Reactant | Tert-butyl 4-(hydroxymethyl)piperidine-1-carboxylate | HCID 2764081 | — |
| Catalyst | HCID 178419074 | HCID 178419074 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | tert-Butyl 4-formylpiperidine-1-carboxylate | HCID 1514430 | 65.5% |
Reaction Steps
To a mixture of the product of Example 1 (23.1 g), 4-methylmorpholine N-oxide (NMO, 18.9 g) and 4A molecular sieves (53.5 g) in DCM (214 mL) was added tetrapropylammonium perruthenate (TPAP, 1.9 g) portion-wise at room temperature. The reaction mixture was stirred at room temperature for 1 h and filtered through a pad of silica gel. Evaporation of solvent gave the title compound as a light yellow oil (15.0 g).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07279491B2 |
| Source dataset | uspto-grants-2007_10 |
| ORD ID | ord-91ac4130c9dd42b38103f825b1facde9 |
| Source note | uspto-grants-2007_10 |