HuagongsheHuagongshe Chemistry Print Report · For research reference only
Penta-1,3-diene → 2-(Bromomethyl)-6-phenylpyridine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Penta-1,3-diene | HCID 15301 | — |
| Reactant | N-bromobutanimide | HCID 67184 | — |
| Reactant | 2-Methyl-6-phenylpyridine | HCID 2762885 | — |
| Product | 2-(Bromomethyl)-6-phenylpyridine | HCID 15229450 | — |
Reaction Steps
2-methyl-6-phenylpyridine, obtainable from 1,3-pentadiene and benzonitirle via the procedure of Janz and McColloch [J. Am. Chem. Soc., 77 (1955), 3413] is treated with N-bromosuccinimide to give 2-bromomethyl-6-phenylpyridine. The bromomethyl compound is treated with 1-methyl-2-cyanopyrrolidine, and the resulting salt is rearranged using sodium amide in liquid ammonia and decyanated with sodium borohydride in ethanol according to the procedures described in Example 1. The product can be purified by distillation.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04155909 |
| Source dataset | uspto-grants-1979_05 |
| ORD ID | ord-c621003fab614ae883bc3b7fce193428 |
| Source note | uspto-grants-1979_05 |