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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1597253Generated: November 1, 2026

4-(Benzyloxy)-5-methoxy-2-nitrobenzamide → HCID 21699258, compound

https://huagongshe.com/reaction/1597253

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-(Benzyloxy)-5-methoxy-2-nitrobenzamideHCID 21699283—
SolventTrifluoroacetic acidHCID 6422—
ProductHCID 21699258HCID 2169925862%

Reaction Steps

4-Benzyloxy-5-methoxy-2-nitrobenzamide (26 g, 91 mmol), (J. Med. Chem. 1977, vol 20, 146-149), was dissolved in TFA and heated at reflux for 2 hours. After cooling the TFA was removed by evaporation and the residue was stirred with 2M sodium hydroxide and insoluble material was removed by filtration. The red aqueous solution was acified to pHl with concentrated hydrochloric acid and allowed to cool back to ambient temperature before collecting the product by filtration. The obtained solid was washed with water and ether and dried in a vacuum oven at 60° C. to give 4-hydroxy-5-methoxy-2-nitrobenzamide (11.04 g, 62%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06294532B1
Source datasetuspto-grants-2001_09
ORD IDord-a3eaa03abf2e4895b3a68be31209ee6f
Source noteuspto-grants-2001_09