HuagongsheHuagongshe Chemistry Print Report · For research reference only
Acetic Acid → Benzyl 1-cyclopentylpiperidine-3-carboxylate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Acetic Acid | HCID 176 | — |
| Reactant | Cyclopentanone | HCID 8452 | — |
| Reactant | Sodium triacetoxyborohydride | HCID 5049666 | — |
| Reactant | Benzyl piperidine-3-carboxylate | HCID 13419237 | — |
| Solvent | 1,2-Dichloroethane | HCID 11 | — |
| Product | Benzyl 1-cyclopentylpiperidine-3-carboxylate | HCID 66844606 | — |
Reaction Steps
The crude amine from the above step was dissolved in 1,2-dichloroethane (15 mL) and cyclopentanone (1.0 mL) was added via syringe. The reaction was allowed to stir for 5 min before the addition of HOAc (0.6 mL) and NaBH(OAc)3 (2.3 g, 10.9 mmol) in one portion. The reaction was allowed to stir for 48 h and then quenched with Na2CO3 (10%, 20 mL) and the reaction was allowed to stir for 1 h before being extracted with DCM (3×50 mL). The combined organics were washed with brine (sat, 200 mL), dried with sodium sulfate, filtered, concentrated to provide 1.3 g of crude oil that was purified by a 120 g Isco normal phase column (100% EtOAc) to give benzyl 1-cyclopentylpiperidine-3-carboxylate as a colorless oil. MS m/z: 288 (M+1).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08163766B2 |
| Source dataset | uspto-grants-2012_04 |
| ORD ID | ord-f1be031d8c264d84902009487d2fb71a |
| Source note | uspto-grants-2012_04 |