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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

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium NitriteHCID 23668193—
ReactantEthyl 6-aminobenzo[d]isoxazole-3-carboxylateHCID 57355978—
CatalystCupric nitrateHCID 18616—
CatalystHCID 178419072HCID 178419072—
SolventWaterHCID 962—
SolventSulfuric AcidHCID 1118—
ProductEthyl 6-hydroxybenzo[d]isoxazole-3-carboxylateHCID 13621661899%

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08106066B2
Source datasetuspto-grants-2012_01
ORD IDord-1e63a6fec163400da8771ee4e39e7b56
Source noteuspto-grants-2012_01