HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ethanol → Ethyl 3-methylpiperidine-4-carboxylate hydrochloride
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ethanol | HCID 702 | — |
| Reactant | Thionyl Chloride | HCID 24386 | — |
| Reactant | 3-Methylpiperidine-4-carboxylic acid hydrochloride | HCID 69169077 | — |
| Product | Ethyl 3-methylpiperidine-4-carboxylate hydrochloride | HCID 51358495 | — |
Reaction Steps
The mixture of 3-methylpiperidine-4-carboxylic acid hydrochloride (3.3 g, 18.4 mmol, 1.0 eq) and SOCl2 (6.6 g, 55.3 mmol, 3.0 equiv) in EtOH (30 mL) was stirred at reflux for 3 h, and then the reaction mixture was concentrated by vacuum to give compound ethyl 3-methylpiperidine-4-carboxylate hydrochloride as a yellow oil which was used for next step. ESI-MS (M+H)+: 172.2.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US09340527B2 |
| Source dataset | uspto-grants-2016_05 |
| ORD ID | ord-ab828ab4f8de435cbeaf92e3a367de83 |
| Source note | uspto-grants-2016_05 |