HuagongsheHuagongshe Chemistry Print Report · For research reference only
Diethyl Ether → Benzyl 4-formylpiperidine-1-carboxylate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Diethyl Ether | HCID 3283 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | Benzyl 4-(hydroxymethyl)piperidine-1-carboxylate | HCID 736490 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | Benzyl 4-formylpiperidine-1-carboxylate | HCID 2776272 | 85.3% |
Reaction Steps
1,1,1-Triacetoxy-1,1-dihydro-1,2-benzoiodoxol-3(1H)-one (1.92 g, 4.53 mmol) was added to a solution of 1-(benzyloxycarbonyl)-4-(hydroxymethyl)piperidine (1.00 g, 4.01 mmol) in CH2Cl2 (20 mL) and the mixture was stirred at RT for 45 min. Ether (75 mL) and 1.3 N NaOH (25 mL) were added and stirring was continued for 15 min. The mixture was transferred to a separatory funnel with additional ether (30 mL) and 1.3 N NaOH (20 mL). The organic layer was separated, washed with saturated aq. NaCl (20 mL, dried (Na2SO4), decanted,and evaporated to give 846 mg of 1-(benzyloxycarbonyl)-4-piperidine carboxaldehyde as a colorless syrup.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06265434B1 |
| Source dataset | uspto-grants-2001_07 |
| ORD ID | ord-4101925129fa40d5a9be27c28aac380e |
| Source note | uspto-grants-2001_07 |