Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1701289Generated: October 30, 2026

HCID 12595981, compound → HCID 13290818, compound

https://huagongshe.com/reaction/1701289

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHCID 12595981HCID 12595981—
ReactantHCID 12617933HCID 12617933—
SolventDichloromethaneHCID 6344—
ProductHCID 13290818HCID 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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04192803
Source datasetuspto-grants-1980_03
ORD IDord-5f16212a64504e278690938a98449316
Source noteuspto-grants-1980_03