HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 393593Generated: October 26, 2026
5-Benzyloxy-2-fluoro-4-methylaniline → 5-Benzyloxy-2-fluoro-4-methylphenol
https://huagongshe.com/reaction/393593
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 5-Benzyloxy-2-fluoro-4-methylaniline | HCID 21991068 | — |
| Reactant | Sodium Nitrite | HCID 23668193 | — |
| Catalyst | Copper oxide | HCID 14829 | — |
| Catalyst | Copper(II) nitrate trihydrate | HCID 9837674 | — |
| Solvent | Acetic Acid | HCID 176 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Sulfuric Acid | HCID 1118 | — |
| Product | 5-Benzyloxy-2-fluoro-4-methylphenol | HCID 21991049 | 27% |
Reaction Steps
A solution of sodium nitrite (1.68 g, 24 mmol) in water (3.5 ml) was added to a solution of 5-benzyloxy-2-fluoro-4-methylaniline (4.7 g, 20 mmol) in acetic acid (25 ml) and 70% sulphuric acid (25 ml) at 10° C. The mixture was stirred at 10° C. for 20 minutes and a solution of copper(II)nitrate trihydrate (481 g, 2 mol) in water (790 ml) followed by copper(II)oxide (3 g, 19 mmol) was added. The mixture was stirred for 3 hours then extracted with ethyl acetate. The organic layer was washed with water, brine, dried (MgSO4) and the solvent removed by evaporation. The residue was purified by column chromatography eluting with petroleum ether/ether (85/15) to give 5-benzyloxy-2-fluoro-4-methylphenol (1.25 g, 27%) as an orange oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06809097B1 |
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| Source dataset | uspto-grants-2004_10 |
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| ORD ID | ord-7113a17c42294fafb4f7216afb6af101 |
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| Source note | uspto-grants-2004_10 |
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