HuagongsheHuagongshe Chemistry Print Report · For research reference only
Methanol → Methyl 3-(piperidin-4-yl)propanoate hydrochloride
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Methanol | HCID 887 | — |
| Reactant | Thionyl Chloride | HCID 24386 | — |
| Reactant | 3-(1-((Tert-butoxy)carbonyl)piperidin-4-yl)propanoic acid | HCID 1512540 | — |
| Product | Methyl 3-(piperidin-4-yl)propanoate hydrochloride | HCID 49761244 | — |
Reaction Steps
To a solution of 4-(2-carboxy-ethyl)-piperidine-1-carboxylic acid tert-butyl ester (1.95 g; 7.58 mmol) in methanol (5 mL) is slowly added thionylchloride (0.99 g; 8.34 mmol) and the reaction mixture is stirred at room temperature for 30 minutes. All volatiles are then removed under high vacuum and the resulting residue triturated with diethyl ether, sucked to dryness and washed (diethyl ether) to afford the desired compound (1.49 g; 7.18 mmol).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US09096524B2 |
| Source dataset | uspto-grants-2015_08 |
| ORD ID | ord-a747ce24015c4862a78853eaa16eb76e |
| Source note | uspto-grants-2015_08 |