HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ammonium formate → 4-(5-Fluoro-2,3-dihydro-benzofuran-7-yl)-piperazine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ammonium formate | HCID 2723923 | — |
| Reactant | 1-Benzyl-4-(5-fluoro-2,3-dihydro-benzofuran-7-yl)-piperazine | HCID 18414130 | — |
| Catalyst | Palladium | HCID 23938 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | 4-(5-Fluoro-2,3-dihydro-benzofuran-7-yl)-piperazine | HCID 18414114 | 75% |
Reaction Steps
A mixture of 1-benzyl-4-(5-fluoro-2,3-dihydro-benzofuran-7-yl)-piperazine (2.06 g, 6.6 mmol), 10% palladium on carbon (0.6 g) and ammonium formate (0.83 g, 13 mmol) in ethanol (20 ml) was allowed to refux for 2 hours. The catalyst was filtered off and the solvent removed under vacuum. Chromatography (10-30% methanol-methylene chloride plus ammonium hydroxide) afforded 1.10 g (75%) of product as a yellow oil; MS EI m/e 222 (M)+.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06313126B1 |
| Source dataset | uspto-grants-2001_11 |
| ORD ID | ord-1d57a4bfbb084577833ad42c3aeca8e9 |
| Source note | uspto-grants-2001_11 |