HuagongsheHuagongshe Chemistry Print Report · For research reference only
Methyl morpholine oxide → tert-Butyl 2-formylpiperidine-1-carboxylate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Methyl morpholine oxide | HCID 82029 | — |
| Reactant | N-Boc-piperidine-2-methanol | HCID 2763853 | — |
| Catalyst | HCID 178419074 | HCID 178419074 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | tert-Butyl 2-formylpiperidine-1-carboxylate | HCID 10656219 | 70% |
Reaction Steps
To a stirred solution of 2-hydroxymethyl-piperidine-1-carboxylic acid tert-butyl ester (0.737 g, 3.4 mmol) in dry CH2Cl2 (10 mL) was added 3 A molecular sieves (1.03 g), N-methylmorpholine N-oxide (0.644 g, 5.5 mmol), and tetrapropylammonium perruthenate (72 mg, 0.21 mmol) and the mixture stirred at room temperature for 3 h. The reaction mixture was purified through a silica gel plug (Hexanes/EtOAc, 70:30 followed by 100:0) to afford the title aldehyde (0.500 g, 70%) as a pale yellow oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07354932B2 |
| Source dataset | uspto-grants-2008_04 |
| ORD ID | ord-c299e239208b4e118cbb682e4d173a69 |
| Source note | uspto-grants-2008_04 |