HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 7495Generated: October 26, 2026
5-Benzyloxy-2-fluoro-4-methylaniline → 5-Benzyloxy-2-fluoro-4-methylphenol
https://huagongshe.com/reaction/7495
Participants
| Role | Name | HCID | Charge |
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| 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
The starting material 5-benzyloxy-2-fluoro-4-methylphenol, was obtained by adding a solution of sodium nitrite (1.68 g, 24mmol) in water (3.5 ml), dropwise, to a solution of 5-benzyloxy-2-fluoro-4-methylaniline (4.7 g, 20 mmol) in acetic acid (82 ml) and 70% sulphuric acid (3.15 ml) cooled at 10° C. The mixture was stirred vigorously for 20 minutes, then a solution of copper(II)nitrate trihydrate (481 g, 2 mol) in water (790 ml) was added, followed by copper(II)oxide (3 g, 19 mmol). After stirring for 3 hours, the mixture was extracted with ethyl acetate. The organic layer was washed with water and then brine, dried (MgSO4) and the solvent evaporated. The resulting oil was purified by flash chromatography using petroleum ether/ether (85/15) as eluent to give 5-benzyloxy-2-fluoro-4-methylphenol as an orange oil (1.25 g, 27%).
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-051c546095a445e08c053b9eb100de40 |
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| Source note | uspto-grants-2006_08 |
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