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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 723165Generated: October 31, 2026

Ammonium Hydroxide → 2-Bromo-5-methoxy-3-methylbenzoic acid

https://huagongshe.com/reaction/723165

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAmmonium HydroxideHCID 14923—
ReactantPotassium PermanganateHCID 516875—
Reactant(2-Bromo-5-methoxy-3-methylphenyl)methanolHCID 15304143—
ReactantSodium BisulfiteHCID 23665763—
SolventAcetoneHCID 180—
Product2-Bromo-5-methoxy-3-methylbenzoic acidHCID 1522736250%

Reaction Conditions

Temperature60 °C

Reaction Steps

A solution of (2-bromo-5-methoxy-3-methyl-phenyl)-methanol ((Example 192: step c) 7.85 g, 34.0 mmol) in acetone (300 mL) was heated to 60° C. and treated over 25 min. with KMnO4 (12.6 g, 79.8 mmol) as an aqueous solution (175 mL). The mixture was heated to 60° C. for an additional 35 min. A saturated aqueous solution of NaHSO3 was added until the solution turned beige in color. Concentrated NH4OH was added to pH 10 and the solids were filtered through a medium porosity fritted funnel. The filtrate was acidified to pH 4 with concentrated HCl, and the solution was extracted with ether (2×200 mL). The combined organic layers were dried over MgSO4 and concentrated in vacuo to afford the product 2-bromo-5-methoxy-3-methyl-benzoic acid (4.15 g, 50%) as a white solid. 1H NMR (MeOD): δ 6.968 (d, 1H, J=2.8 Hz), 6.775 (d, 1H, J=3.2 Hz), 3.776 (s, 3H), 2.352 (s, 3H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07138530B2
Source datasetuspto-grants-2006_11
ORD IDord-da7d7d9b90234a71b0721e28c60b711e
Source noteuspto-grants-2006_11