HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ethyl formate → 3-(3-Methoxyphenyl)-1-methyl-5-phenylpiperidin-4-one
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ethyl formate | HCID 8025 | — |
| Reactant | 4(1H)-Pyridinone, 3-(3-methoxyphenyl)-1-methyl-5-phenyl- | HCID 181234 | — |
| Reactant | Methylamine hydrochloride | HCID 6364545 | — |
| Reactant | 1-(3-Methoxyphenyl)-3-phenylpropan-2-one | HCID 20317061 | — |
| Reactant | Aluminium lithium hydride | HCID 21226445 | — |
| Product | 3-(3-Methoxyphenyl)-1-methyl-5-phenylpiperidin-4-one | HCID 20317095 | — |
Reaction Steps
A 54 g. portion of 1-(3-methoxyphenyl)-3-phenyl-2-propanone was reacted with ethyl formate and methylamine hydrochloride as described in Examples 1-3 to prepare 10 g. of 3-(3-methoxyphenyl)-1-methyl-5-phenyl-4(1H)-pyridinone, which was reduced with 2 g. of lithium aluminum hydride. The reaction mixture was worked up as in the examples above and chromatographed over a silica gel column. About 1.4 g. of a mixture of the compounds of Examples 24 and 25 was obtained, an oil which was identified by mass spectroscopy as having a molecular weight of 293. About 1.3 g. of the piperidinone of Example 26 was recovered, which had an indicated molecular weight of 295 by mass spectroscopy.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04065290 |
| Source dataset | uspto-grants-1977_12 |
| ORD ID | ord-f0600dff8310468981bd6fac2756262a |
| Source note | uspto-grants-1977_12 |