HuagongsheHuagongshe Chemistry Print Report · For research reference only
4-Fluoro-1-benzofuran-3(2H)-one → 2,3-Dihydro-1-benzofuran-3-amine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 4-Fluoro-1-benzofuran-3(2H)-one | HCID 45122651 | — |
| Reactant | HCID 72368497 | HCID 72368497 | — |
| Catalyst | Palladium | HCID 23938 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | 2,3-Dihydro-1-benzofuran-3-amine | HCID 13778152 | — |
Reaction Steps
To the solution of benzofuran-3(2H)-one oxime (1.0 g, obtained from commercially available benzofuran-3(2H)-one via the procedure outlined for the synthesis of 4-fluorobenzofuran-3(2H)-one oxime from 4-fluorobenzofuran-3(2H)-one) in 50 mL MeOH, 10% Palladium on active carbon (0.1 g) was added. The mixture was evacuated then filled with H2 three times. Finally the oxime was reduced under a H2 balloon for 24 hours. The mixture was filtered through a pad of celite, and the cake was washed with MeOH twice. After removing the solvents under vacuum, 0.99 g brown-yellow residue was obtained as the desired amine. 1H NMR (300 MHz, CDCl3): δ 7.32 (d, 1H), 7.19 (t, 1H), 6.94 (t, 1H), 6.82 (d, 1H), 4.5-4.7 (m, 1H), 4.64 (s, 1H), 4.1-4.2 (m, 1H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07884109B2 |
| Source dataset | uspto-grants-2011_02 |
| ORD ID | ord-5623af2d310e4d579f37e7193c7c5ac7 |
| Source note | uspto-grants-2011_02 |