HuagongsheHuagongshe Chemistry Print Report · For research reference only
Acetic Anhydride → Methyl 1-acetyl-4-oxopiperidine-3-carboxylate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Acetic Anhydride | HCID 7918 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Methyl 4-oxopiperidine-3-carboxylate hydrochloride | HCID 2724028 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | Methyl 1-acetyl-4-oxopiperidine-3-carboxylate | HCID 14143329 | 59.3% |
Reaction Steps
Methyl 4-oxo-3-piperidinecarboxylate hydrochloride (10 g, 51.65 mmol) was dissolved in dichloromethane (130 mL). Triethylamine (7.20 mL, 51.65 mmol) was added followed by acetic anhydride (4.87 mL, 51.65 mmol). The reaction mixture was stirred at room temperature for 2 h. The organic phase was washed with water, dried over MgSO4, filtered and concentrated to give methyl 1-acetyl-4-oxopiperidine-3-carboxylate (6.10 g, 59.3%), which was used in the next step as such.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08188101B2 |
| Source dataset | uspto-grants-2012_05 |
| ORD ID | ord-978d97d6eed743db870ed37c272c7d22 |
| Source note | uspto-grants-2012_05 |