HuagongsheHuagongshe Chemistry Print Report · For research reference only
Methanol → N-acetyl-4-(2-methoxy-n-propoxy)piperidine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Methanol | HCID 887 | — |
| Reactant | N-acetyl-4-allyloxypiperidine | HCID 12920043 | — |
| Product | N-acetyl-4-(2-methoxy-n-propoxy)piperidine | HCID 20306010 | — |
Reaction Steps
This compound was prepared similarly to Example F, starting from N-acetyl-4-allyloxypiperidine and mercuric acetate in methanol. To improve the conversion of starting material to product the mercuric acetate/methanol treatment was repeated twice to give N-acetyl-4-(2-methoxy-n-propoxy)piperidine, which was hydrolyzed in sodium hydroxide and methanol solution to give 4-(2-methoxy-n-propoxy)piperidine. A sample was characterized as the oxalate salt, m.p. 89°-91° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04237138 |
| Source dataset | uspto-grants-1980_12 |
| ORD ID | ord-ec622337630941358cf0f07033a81667 |
| Source note | uspto-grants-1980_12 |