HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ammonium formate → Ethyl 3-amino-2-hydroxybenzoate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ammonium formate | HCID 2723923 | — |
| Reactant | Ethyl 2-hydroxy-3-nitrobenzoate | HCID 12157235 | — |
| Reactant | HCID 178418361 | HCID 178418361 | — |
| Catalyst | Palladium | HCID 23938 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | Ethyl 3-amino-2-hydroxybenzoate | HCID 22096614 | 99.3% |
Reaction Steps
To a solution of 2-hydroxy-3-nitrobenzoic acid ethyl ester 8.4 g (40 mmol) of step 1 in methanol 100 mL was added 5% Pd/C 0.84 g, after which the reactor was filled hydrogen gas, followed by stirring at room temperature for 5 hrs. Ammoniumformate 0.5 g was added to the reaction mixture before re-filling with hydrogen gas and re-stirring at room temperature for 24 hrs. The catalyst was removed by celite filtration, followed by vacuum concentration to afford the title compound 7.2 g (yield 99%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08026235B1 |
| Source dataset | uspto-grants-2011_09 |
| ORD ID | ord-b8fdd6f131f24842af3a96005482d925 |
| Source note | uspto-grants-2011_09 |