HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2115646Generated: October 29, 2026
Hydrochloric Acid → 2-HYDROXY-6-NITROBENZALDEHYDE
https://huagongshe.com/reaction/2115646
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | HCID 22258788 | HCID 22258788 | — |
| Solvent | Ethanol | HCID 702 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Solvent | 1,4-Dioxane | HCID 31275 | — |
| Product | 2-HYDROXY-6-NITROBENZALDEHYDE | HCID 10953909 | — |
Reaction Steps
To a stirred solution of 4-ethoxy-5-nitro-4H-1,3-benzodioxine (5.80 g, 25.755 mmol) in ethanol (15 mL) and THF (10 mL) was added 4N HCl in 1,4-dioxane (20 mL). The mixture was stirred at 60° C. for 6 hrs and 90° C. for 6 hrs. After cooled to room temperature, the reaction mixture was diluted with water and extracted with ethyl acetate. The organic phase was dried over magnesium sulfate, filtered and concentrated under reduced pressure. The residue was purified by column chromatography on silica gel (hexane/ethyl acetate=9/1) to give 2-hydroxy-6-nitrobenzaldehyde as a pale yellow oil (4.450 g, yield; quant.).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07435743B2 |
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| Source dataset | uspto-grants-2008_10 |
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| ORD ID | ord-8c5f614a35124e74aa3c8ff72a75c7ba |
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| Source note | uspto-grants-2008_10 |
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