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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1478468Generated: October 30, 2026

Potassium Hydroxide → 4-Tert-butoxy-3-methoxy-benzoic acid

https://huagongshe.com/reaction/1478468

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium HydroxideHCID 14797—
ReactantPotassium PermanganateHCID 516875—
Reactant4-Tert-butoxy-3-methoxybenzaldehydeHCID 15439417—
Solvent1,4-DioxaneHCID 31275—
Product4-Tert-butoxy-3-methoxy-benzoic acidHCID 5855122949%

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09403839B2
Source datasetuspto-grants-2016_08
ORD IDord-4247736505854f188a508abb571f5fa1
Source noteuspto-grants-2016_08