HuagongsheHuagongshe Chemistry Print Report · For research reference only
Methyl iodide → HCID 14330045, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Methyl iodide | HCID 6328 | — |
| Reactant | Pyridinium, 1-methyl-, iodide (1:1) | HCID 13596 | — |
| Reactant | Sodium borohydride | HCID 4311764 | — |
| Reactant | HCID 14330044 | HCID 14330044 | — |
| Product | HCID 14330045 | HCID 14330045 | — |
Reaction Steps
Employing the general methods of Examples 4 and 6 above, 10 g (47.3 mmol) of 3-phenyl-1-(3-pyridinyl)-1-propanone were first converted by the action of methyl iodide to the N-methylpyridinium iodide and then reduced by the action of sodium borohydride to produce 3-phenyl-1-(1,2,5,6-tetrahydro-1-methyl-3-pyridinyl)-1-propanone which was isolated as the hydrochloride salt (5.2 g, 58%), mp 195°-197° C. cl EXAMPLE 8
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04798841 |
| Source dataset | uspto-grants-1989_01 |
| ORD ID | ord-6e2ffdc520364a2da25d5cc1774d23bd |
| Source note | uspto-grants-1989_01 |