Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Sodium Methoxide | HCID 10942334 | — |
| Reactant | HCID 53763119 | HCID 53763119 | — |
| Product | HCID 53884800 | HCID 53884800 | 130.9% |
Reaction Steps
2-p-Chlorobenzyl-6-cyanopyridine (1.69 g, 0.0074 moles) was added to a solution of sodium methoxide [prepared by dissolving sodium metal (0.19 g, 0.0081 gram atoms) in methanol (20 ml)] under nitrogen, and the mixture stirred at 20° C. for 17 hours. The methanol was evaporated, the residue taken up in chloroform, neutralised with acetic acid and the precipitate filtered off on HYFLO. Concentration of the filtrate gave methyl 6-p-chlorobenzyl-2-picoline imidate (1.20 g, 62%) which was used in the next stage without further purification.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US05185339 |
|---|
| Source dataset | uspto-grants-1993_02 |
|---|
| ORD ID | ord-32dadcce765d4e4b84d4f5603c2be7b6 |
|---|
| Source note | uspto-grants-1993_02 |
|---|