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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

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 numberUS09365588B2
Source datasetuspto-grants-2016_06
ORD IDord-b2e1776fab20486f945431931130fbec
Source noteuspto-grants-2016_06