HuagongsheHuagongshe Chemistry Print Report · For research reference only
Trimethyl orthoformate → 1-Acetyl-4,4-dimethoxy-piperidine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Trimethyl orthoformate | HCID 9005 | — |
| Reactant | N-Acetyl-4-piperidone | HCID 122563 | — |
| Catalyst | p-Toluenesulfonic acid monohydrate | HCID 521998 | — |
| Catalyst | Sodium Methoxide | HCID 10942334 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | 1-Acetyl-4,4-dimethoxy-piperidine | HCID 12653646 | 89.2% |
Reaction Steps
A solution of 1-acetyl-4-piperidone (17.0 g, 121 mmol), trimethyl orthoformate (26.4 mL, 241 mmol) and para-toluenesulfonic acid monohydrate (80 mg, 0.42 mmol) in dry methanol (34 mL) was refluxed for one hour. Then 1.0 M methanolic NaOMe (0.42 mL, 0.42 mmol) and excess of methanol and trimethyl orthoformate were removed by distillation (atmospheric pressure). Further distillation under reduced pressure afforded 1-acetyl-4,4-dimethoxy-piperidine (20.2 g, 89%) 1H NMR (DMSO) δ 3.45-3.32 (m, 4H), 3.10 (s, 6H), 1.99 (s, 3H), 1.72-1.62 (m, 2H), 1.61-1.52 (m, 2H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08338431B2 |
| Source dataset | uspto-grants-2012_12 |
| ORD ID | ord-4a56d7b9dea5446f82ab7ca68dcaa477 |
| Source note | uspto-grants-2012_12 |