HuagongsheHuagongshe Chemistry Print Report · For research reference only
Tetrahydrofuran toluene → Ethyl 4-(4-hydroxy-1-piperidyl)-4-methyl-piperidine-1-carboxylate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Tetrahydrofuran toluene | HCID 22635083 | — |
| Reactant | Ethyl 4-cyano-4-(4-hydroxy-1-piperidyl)piperidine-1-carboxylate | HCID 57619806 | — |
| Reactant | HCID 178418689 | HCID 178418689 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | Ethyl 4-(4-hydroxy-1-piperidyl)-4-methyl-piperidine-1-carboxylate | HCID 57619818 | 65.5% |
Reaction Steps
To a stirred solution of ethyl 4-cyano-4-(4-hydroxy-1-piperidyl)piperidine-1-carboxylate (2.45 g, 8.69 mmol) in THF (20 mL) was added a 1.4 M solution of MeMgBr in toluene/THF (18.6 mL, 26.1 mmol) at 0° C., and the mixture was stirred at room temperature for 12 h. The reaction was then quenched with saturated aqueous ammonium chloride, and the mixture was extracted with dichloromethane (2×25 mL). The combined extracts were concentrated in vacuo to afford the title compound (1.54 g, 65%), which was used in the next step without further purification. MS (M+1): 271.26.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08119661B2 |
| Source dataset | uspto-grants-2012_02 |
| ORD ID | ord-d6f4eb0725dd49f28bcc43cf5affb39a |
| Source note | uspto-grants-2012_02 |