HuagongsheHuagongshe Chemistry Print Report · For research reference only
Tert-butyl 2-nitrobenzoate → tert-Butyl 2-aminobenzoate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Tert-butyl 2-nitrobenzoate | HCID 4860715 | — |
| Catalyst | HCID 178418390 | HCID 178418390 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | tert-Butyl 2-aminobenzoate | HCID 3430448 | 887.3% |
Reaction Steps
A mixture of tert-butyl 2-nitrobenzoate (2.1 g.) in methanol (200 ml.) was hydrogenated over palladium-carbon (2 g.) with shaking at atmospheric pressure and room temperature for 3.5 hours. The reaction mixture was filtered to remove the catalyst and then evaporated. To the residue were successively added diethyl ether and an aqueous solution of sodium chloride followed by shaking. The organic layer was separated, dried over magnesium sulfate, treated with activated charcoal and then evaporated to give an oil of the title compound (16.13 g.).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04288435 |
| Source dataset | uspto-grants-1981_09 |
| ORD ID | ord-d28a929dca7b4865ac8a4c50a579a59c |
| Source note | uspto-grants-1981_09 |