HuagongsheHuagongshe Chemistry Print Report · For research reference only
Benzene → HCID 12640216, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Benzene | HCID 241 | — |
| Reactant | 3-Chlorobenzaldehyde | HCID 11477 | — |
| Reactant | Methyl 5-aminopyridine-2-carboxylate | HCID 12457877 | — |
| Solvent | Water | HCID 962 | — |
| Product | HCID 12640216 | HCID 12640216 | — |
Reaction Steps
The starting material is prepared as follows: the mixture of 30.44 g of 5-aminopyridine-2-carboxylic acid methyl ester, 30.9 g of m-chlorobenzaldehyde, and 400 ml of benzene is refluxed for 3 days on a water-separating trap. The initial suspension eventually becomes a pale yellow solution, which is evaporated. The residual yellow solid is recrystallized from benzene-ethyl acetate-diethyl ether, to yield the 5-(m-chlorobenzylideneamino)-pyridine-2-carboxylic acid methyl ester melting at 139°-142°.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04273779 |
| Source dataset | uspto-grants-1981_06 |
| ORD ID | ord-8bcc0ee4fbdc4441a9a9e3dd765e054d |
| Source note | uspto-grants-1981_06 |