HuagongsheHuagongshe Chemistry Print Report · For research reference only
Methanol → Methyl 4-(piperidin-2-yl)butanoate hydrochloride
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Methanol | HCID 887 | — |
| Reactant | Thionyl Chloride | HCID 24386 | — |
| Reactant | 4-(Piperidin-2-yl)butanoic acid--hydrogen chloride (1/1) | HCID 12416327 | — |
| Product | Methyl 4-(piperidin-2-yl)butanoate hydrochloride | HCID 66772062 | 45% |
Reaction Steps
A solution of 4-(2-piperidinyl)butanoic acid hydrochloride (5.95 g, 34.8 mmol) in methanol (104 ml) was cooled to 0° C. Thionyl chloride (7.54 ml, 104.3 mmol) was slowly added at this temperature. The reaction mixture was heated under reflux for 12 h. The solvent was evaporated off under reduced pressure. The residue was suspended in ethyl acetate and the suspension was heated under reflux. The suspension was filtered hot. A white precipitate precipitates out in the filtrate, and was filtered out and dried under reduced pressure to give the product methyl 4-(piperidine-2-yl)butanoate hydrochloride (2) (3.49 g, 45%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08318769B2 |
| Source dataset | uspto-grants-2012_11 |
| ORD ID | ord-1bfeece9c79545f4ba90cda4d6079ccd |
| Source note | uspto-grants-2012_11 |