HuagongsheHuagongshe Chemistry Print Report · For research reference only
Acetic Anhydride → HCID 15291737, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Acetic Anhydride | HCID 7918 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | 4-(Aminomethyl)-1-methylpiperidin-4-ol | HCID 6484262 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | HCID 15291737 | HCID 15291737 | 91% |
Reaction Steps
4-aminomethyl-4-hydroxy-1-methylpiperidine (2.95 g, 0.02 mole), potassium carbonate (6.5 g, 0.047 mole) and acetic anhydride (8.5 g, 0.08 mole) in methanol were mixed at room temperature for two hours. Sodium hydroxide was added for neutralization and the solution extracted with chloroform. After evaporation, a yellow oil was obtained which was identified as 4-acetamidomethyl-4-hydroxy--1-methylpiperidine (3.4 g, 0.018 mole, 91% yield).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05534520 |
| Source dataset | uspto-grants-1996_07 |
| ORD ID | ord-754de210565146cdaccae396e19092bf |
| Source note | uspto-grants-1996_07 |