HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ethanol → 4-(Benzyloxy)-2-fluoroaniline
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ethanol | HCID 702 | — |
| Reactant | Tetrahydrofuran | HCID 8028 | — |
| Reactant | Sodium Dithionite | HCID 24489 | — |
| Reactant | 4-Benzyloxy-2-fluoro-1-nitrobenzene | HCID 22180704 | — |
| Solvent | Water | HCID 962 | — |
| Product | 4-(Benzyloxy)-2-fluoroaniline | HCID 11499809 | 42% |
Reaction Steps
A solution of Na2S2O4 (34.8 g, 200 mmol) in H2O (200 mL) was added to a mixture of 4-(benzyloxy)-2-fluoro-1-nitrobenzene (16.0 g, 64.7 mmol), THF (150 mL), and EtOH (150 mL), and the mixture was stirred for 30 min at room temperature. The reaction mixture was poured into water and extracted with AcOEt. The extract was washed with water and brine, dried over MgSO4, and concentrated under reduced pressure. The residue was purified by basic silica gel column chromatography eluting with hexane/AcOEt (1/1) to give the title compound (5.84 g, 42% yield) as a light brown oil: 1H NMR (300 MHz, CDCl3): δ ppm 3.42 (2H, brs), 4.97 (2H, s), 6.60 (1H, ddd, J=1.1, 2.6, 8.7 Hz), 6.67-6.74 (2H, m), 7.28-7.43 (5H, m).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08513251B2 |
| Source dataset | uspto-grants-2013_08 |
| ORD ID | ord-d880f34b30ad42cb8429aa6fa28e3621 |
| Source note | uspto-grants-2013_08 |