HuagongsheHuagongshe Chemistry Print Report · For research reference only
Cyanide → 4-Cyanopyridine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Cyanide | HCID 5975 | — |
| Reactant | HCID 22168441 | HCID 22168441 | — |
| Product | 4-Cyanopyridine | HCID 7506 | — |
| Product | 3-Methylpyridine-2-carbonitrile | HCID 819928 | — |
Reaction Steps
It has been reported by Fife et al., Heterocycles 22:1121-4(1984) that 3-methyl-1-methoxypyridinium methylsulfate reacted with cyanide ion to give 3-methyl-2-cyanopyridine and "high percentages" of the 4-cyanopyridine isomer. In Table 1 on page 1122, Fife et al. reported that the 4-cyano compound was gobtained in 69% yield and 3-methyl-2-cyanopyridine was obtained in 24% yield.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04843163 |
| Source dataset | uspto-grants-1989_06 |
| ORD ID | ord-e20f50c5acee44ae99940512b8ec0dd6 |
| Source note | uspto-grants-1989_06 |