HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2204166Generated: October 30, 2026
Potassium Hydroxide → 4-Tert-butoxy-3-methoxy-benzoic acid
https://huagongshe.com/reaction/2204166
Participants
| Role | Name | HCID | Charge |
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| Reactant | Potassium Hydroxide | HCID 14797 | — |
| Reactant | Potassium Permanganate | HCID 516875 | — |
| Reactant | 4-Tert-butoxy-3-methoxybenzaldehyde | HCID 15439417 | — |
| Solvent | 1,4-Dioxane | HCID 31275 | — |
| Product | 4-Tert-butoxy-3-methoxy-benzoic acid | HCID 58551229 | 49% |
Reaction Steps
4-tert-Butoxy-3-methoxybenzaldehyde (130 mg, 0.62 mmol) was suspended in a mixture of dioxane (520 μL) and potassium hydroxide (6.5 mL of 0.20 M, 1.3 mmol). KMnO4 (150 mg, 0.93 mmol) was added and the reaction was stirred vigorously for 16 h. The reaction mixture was filtered and then concentrated to 3 mL. Hydrochloric acid (1M, 4 mL) was added and the resulting precipitate was filtered (after standing for 15 minutes) and washed with 1M HCl and a small amount of water to yield 4-tert-butoxy-3-methoxy-benzoic acid (68 mg, 49%) as a white solid. Rf=0.23 (SiO2, 40% ethyl acetate in hexanes); ESI-MS m/z calc. 224.1, found 225.2 (M+1)+. Retention time: 1.66 minutes (3 min run). 1H NMR (400 MHz, DMSO) δ 12.80 (s, 1H), 7.66-7.41 (m, 2H), 7.09 (d, J=8.8 Hz, 1H), 3.78 (s, 3H), 1.32 (s, 9H).
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-b2e1776fab20486f945431931130fbec |
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| Source note | uspto-grants-2016_06 |
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