HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2204169Generated: November 1, 2026
Potassium Hydroxide → HCID 58551608, compound
https://huagongshe.com/reaction/2204169
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Potassium Hydroxide | HCID 14797 | — |
| Reactant | Potassium Permanganate | HCID 516875 | — |
| Reactant | HCID 58086339 | HCID 58086339 | — |
| Solvent | 1,4-Dioxane | HCID 31275 | — |
| Product | HCID 58551608 | HCID 58551608 | 78% |
Reaction Steps
2-Fluoro-5-methoxy-4-(2-methoxyethoxy)benzaldehyde (0.36 g, 1.6 mmol) was suspended in a mixture of dioxane (1.5 mL) and KOH (16 mL of 0.2 M, 3.2 mmol). KMnO4 (370 mg, 2.4 mmol) was added and the mixture was stirred vigorously for 30 minutes. The reaction mixture was filtered and the filtrate was concentrated to 10 mL (blue soln). HCl (4M, mL) was added and the resulting precipitate was filtered and washed with 1M HCl and then water (1 mL) to yield 2-fluoro-5-methoxy-4-(2-methoxyethoxy)benzoic acid (300 mg, 78%) as a white solid. ESI-MS m/z calc. 244.1, found 245.1 (M+1)F. Retention time: 1.01 minutes (3 min run). 1H NMR (400 MHz, DMSO) δ 12.96 (s, 1H), 7.30 (d, J=7.0 Hz, 1H), 6.98 (d, J=12.5 Hz, 1H), 4.20-4.13 (m, 2H), 3.78 (s, 3H), 3.71-3.63 (m, 2H), 3.31 (s, 3H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09365588B2 |
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| Source dataset | uspto-grants-2016_06 |
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| ORD ID | ord-e82172b2601d476089146e4356a90163 |
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| Source note | uspto-grants-2016_06 |
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