HuagongsheHuagongshe Chemistry Print Report · For research reference only
p-Toluenesulfonic acid → Methyl 3-anilinopyrazine-2-carboxylate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | p-Toluenesulfonic acid | HCID 6101 | — |
| Reactant | Aniline | HCID 6115 | — |
| Reactant | Methyl 3-bromopyrazine-2-carboxylate | HCID 13318551 | — |
| Solvent | Water | HCID 962 | — |
| Product | Methyl 3-anilinopyrazine-2-carboxylate | HCID 13370930 | — |
Reaction Steps
A mixture of 9.5 g. of methyl 2-bromo-3-pyrazine carboxylate, 8.2 g. of aniline, 0.5 g. of p-toluene sulfonic acid and 100 ml. of water was stirred and refluxed for two hours. The reaction mixture was poured on ice, extracted with ethyl acetate, the organic extracts were dried and concentrated to yield an oil. The crude residue was eluted on a silica gel column with ethyl acetate-hexane (1:2) yielding the product of this example as a yellow solid, m.p. 72°-75° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04680297 |
| Source dataset | uspto-grants-1987_07 |
| ORD ID | ord-fd6a54d3e1b6482bac61b663f4580f05 |
| Source note | uspto-grants-1987_07 |