HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 424637Generated: October 26, 2026
Sodium Nitrite → Ethyl 6-hydroxybenzo[d]isoxazole-3-carboxylate
https://huagongshe.com/reaction/424637
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Sodium Nitrite | HCID 23668193 | — |
| Reactant | Ethyl 6-aminobenzo[d]isoxazole-3-carboxylate | HCID 57355978 | — |
| Catalyst | Cupric nitrate | HCID 18616 | — |
| Catalyst | HCID 178419072 | HCID 178419072 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Sulfuric Acid | HCID 1118 | — |
| Product | Ethyl 6-hydroxybenzo[d]isoxazole-3-carboxylate | HCID 136216618 | 99% |
Reaction Steps
Ethyl 6-aminobenzo[d]isoxazole-3-carboxylate (2.43 mmol) was diluted with a solution of sulfuric acid (2.5 mL) in water (2.5 mL) and the resulting mixture was maintained at rt for 30 min. A solution of sodium nitrite (2.67 mmol) in water (2.5 ml) was added dropwise at 0° C. and the resulting mixture was maintained for 30 min at 0° C. This aqueous solution was added to a cold (0° C.) solution of copper (II) nitrate (149 mmol) in water (80 mL) and the reaction mixture was allowed to warm to rt. After 5 min., copper (I) oxide (2.78 mmol) was added to the mixture and the reaction mixture was maintained for 1 h at rt. The reaction mixture was extracted with ethyl acetate (3×100 mL) and the combined organic layers were dried (magnesium sulfate) and concentrated to provide crude ethyl 6-hydroxybenzo[d]isoxazole-3-carboxylate in 99% yield as a brown oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08106066B2 |
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| Source dataset | uspto-grants-2012_01 |
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| ORD ID | ord-1e63a6fec163400da8771ee4e39e7b56 |
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| Source note | uspto-grants-2012_01 |
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