HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 7496Generated: October 26, 2026
5-Benzyloxy-2-fluoro-4-methylnitrobenzene → 5-Benzyloxy-2-fluoro-4-methylaniline
https://huagongshe.com/reaction/7496
Participants
| Role | Name | HCID | Charge |
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| Reactant | 5-Benzyloxy-2-fluoro-4-methylnitrobenzene | HCID 21991057 | — |
| Catalyst | Iron | HCID 23925 | — |
| Solvent | Acetic Acid | HCID 176 | — |
| Solvent | Water | HCID 962 | — |
| Product | 5-Benzyloxy-2-fluoro-4-methylaniline | HCID 21991068 | 87.7% |
Reaction Steps
The starting material, 5-benzyloxy-2-fluoro-4-methylaniline, was obtained by adding iron powder (2.88 g, 51 mmol), in portions, to a solution of 5-benzyloxy-2-fluoro-4-methylnitrobenzene (4.8 g, 18 mmol) in acetic acid (33 ml) and water (5.7 ml), at ambient temperature. The mixture was heated and after stirring at 100° C. for 10 minutes, it was cooled and partitioned between ethyl acetate and water. The organic layer was washed with water, aqueous saturated sodium carbonate solution and then brine, dried (MgSO4) and the solvent evaporated. The residue was purified by flash chromatography using petroleum ether/ethyl acetate (8/2) as eluent to give 5-benzyloxy-2-fluoro-4-methylaniline (3.65 g, 87%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07087602B2 |
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| Source dataset | uspto-grants-2006_08 |
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| ORD ID | ord-c8db631387344b1d934a549994ef9606 |
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| Source note | uspto-grants-2006_08 |
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