HuagongsheHuagongshe Chemistry Print Report · For research reference only
4-Nitro-3-(tetrahydrofuran-3-yloxy)-benzamide → 4-Amino-3-(tetrahydrofuran-3-yloxy)-benzamide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 4-Nitro-3-(tetrahydrofuran-3-yloxy)-benzamide | HCID 59225963 | — |
| Catalyst | Palladium | HCID 23938 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | 4-Amino-3-(tetrahydrofuran-3-yloxy)-benzamide | HCID 59225964 | 104.1% |
Reaction Steps
To a solution of 4-nitro-3-(tetrahydrofuran-3-yloxy)-benzamide (4.77 g, 18.15 mmol) in ethanol (200 ml) was added 10% palladium on carbon (0.5 g, 10% w/w) and the flask rinsed with an additional portion of ethanol (20 ml). The reaction was then purged with a nitrogen atmosphere, placed under a H2 (g) atmosphere and stirred at room temperature for 18 hours. The reaction was then purged with N2 (g) and filtered through a celite pad. The pad was washed with ethanol (100 ml) and the filtrate concentrated to dryness in vacuo to give the title compound as a white solid (4.22 g, 18.9 mmol, 100% corrected). LCMS: [M+H]+=223, Rt=1.01 min, 100% purity
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08633201B2 |
| Source dataset | uspto-grants-2014_01 |
| ORD ID | ord-59d595e5ea21420b91ff3bcec5562e6f |
| Source note | uspto-grants-2014_01 |