HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ethanol → 2-Methyl-5-benzofuranamine oxalate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ethanol | HCID 702 | — |
| Reactant | Ammonium formate | HCID 2723923 | — |
| Reactant | 2-Methyl-5-nitrobenzofuran | HCID 4487453 | — |
| Catalyst | Palladium | HCID 23938 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 2-Methyl-5-benzofuranamine oxalate | HCID 21696864 | — |
Reaction Steps
To a 35° C. mixture of 50 g of 2-methyl-5-nitrobenzofuran, ethanol (250 mL), THF (250 mL) and wet 10% Pd/C (4 g) was added ammonium formate (53.4 g, 0.85 mol) over 50 min. After an additional 4 h, the reaction was cooled to room temperature and filtered through Celite. The filtrate was concentrated and the residue was taken up in methyl t-butyl ether (415 mL). This mixture was filtered and a solution of oxalic acid (25.4 g) in methanol (80 mL) was added dropwise. The precipitate was stirred for 2 h, collected, washed with methanol/TBME and dried to provide 2-methyl-5-benzofuranamine oxalate.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06297233B1 |
| Source dataset | uspto-grants-2001_10 |
| ORD ID | ord-08551cd065bc4b02884dc079f22ef35c |
| Source note | uspto-grants-2001_10 |