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
Acetyl chloride was slowly added dropwise to a solution of tert-butyl 2-(4-methoxy-4-oxobutyl)piperidine-1-carboxylate (3) (25.67 g, 89.9 mmol) in methanol. The reaction mixture was stirred at room temperature for 5 h. The complete reaction was checked by means of TLC. When the reaction was complete, the reaction mixture was concentrated under reduced pressure to obtain methyl 4-(piperidine-2-yl)butanoate hydrochloride (4) (20.14 g, 100%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08318769B2 |
| Source dataset | uspto-grants-2012_11 |
| ORD ID | ord-3609fd042a8b433fad0ebe890b2cccec |
| Source note | uspto-grants-2012_11 |