HuagongsheHuagongshe Chemistry Print Report · For research reference only
2-Amino-5-nitrobenzoic acid → 5-Nitro-2-(pyrrol-1-yl)benzoic acid
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 2-Amino-5-nitrobenzoic acid | HCID 12032 | — |
| Reactant | 2,5-Dimethoxytetrahydrofuran | HCID 79098 | — |
| Solvent | Acetic Acid | HCID 176 | — |
| Product | 5-Nitro-2-(pyrrol-1-yl)benzoic acid | HCID 12196200 | 73% |
Reaction Steps
A mixture of 2-amino-5-nitrobenzoic acid (475 mg), 2,5-dimethoxytetrahydrofuran (345 mg) and acetic acid (10 ml) was heated under reflux for 3 hours and then concentrated at reduced pressure. Brine was added to the resulting residue and the mixture was extracted with ethyl acetate. The organic layer was dried with anhydrous sodium sulfate and then concentrated at reduced pressure. The resulting residue was purified by silica gel column chromatography (eluent; ethyl acetate:n-hexane=1:1) to give the titled compound (yield, 73%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06414005B1 |
| Source dataset | uspto-grants-2002_07 |
| ORD ID | ord-70e317d51d3048dab986c281029323ce |
| Source note | uspto-grants-2002_07 |