HuagongsheHuagongshe Chemistry Print Report · For research reference only
Acetyl chloride → Methyl 4-(piperidin-2-yl)butanoate hydrochloride
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Acetyl chloride | HCID 6367 | — |
| Reactant | Tert-butyl 2-(4-methoxy-4-oxobutyl)piperidine-1-carboxylate | HCID 57904248 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | Methyl 4-(piperidin-2-yl)butanoate hydrochloride | HCID 66772062 | 100% |
Reaction Steps
To a solution of tert-Butyl-2-(4-methoxy-4-oxobutyl)piperidine-1-carboxylate (3) (25.67 g, 89.9 mmol) in Methanol was added dropwise acetyl chloride. The reaction mixture was stirred for 5 h at room temperature. The completion of the reaction was controlled via Thin-layer chromatography. After completion the reaction mixture was evaporated in vacuum to give Methyl 4-(piperidin-2-yl)butanoate hydrochloride (4) (20.14 g, 100%)
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08268814B2 |
| Source dataset | uspto-grants-2012_09 |
| ORD ID | ord-326e635a29d846eab8e5aaec76825605 |
| Source note | uspto-grants-2012_09 |