HuagongsheHuagongshe Chemistry Print Report · For research reference only
HCID 12595981, compound → HCID 13290818, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | HCID 12595981 | HCID 12595981 | — |
| Reactant | HCID 12617933 | HCID 12617933 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 13290818 | HCID 13290818 | — |
Reaction Steps
1-(o-Aminobenzyl)-2-pyrrolecarboxylic acid, prepared by hydrolysis of 1-(o-aminobenzyl)-2-pyrrolecarbonitrile (Example 1) with potassium hydroxide (Example 1), is heated above its melting point for several minutes (245°-250° C.). After the evolution of gases ceases the residue is cooled, taken up in methylene chloride, and a small amount of precipitate is filtered. The filtrate is evaporated and the residue is crystallized with the aid of petroleum ether to give 1-(o-aminobenzyl)pyrrole.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04192803 |
| Source dataset | uspto-grants-1980_03 |
| ORD ID | ord-5f16212a64504e278690938a98449316 |
| Source note | uspto-grants-1980_03 |