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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 389967Generated: October 30, 2026

Potassium Hydroxide → 2-Hydroxy-5-isopropyl-4-(methoxymethyloxy)benzoic acid

https://huagongshe.com/reaction/389967

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium HydroxideHCID 14797—
ReactantMethyl 2-hydroxy-5-isopropyl-4-(methoxymethyloxy)benzoateHCID 58236463—
SolventMethanolHCID 887—
SolventWaterHCID 962—
Product2-Hydroxy-5-isopropyl-4-(methoxymethyloxy)benzoic acidHCID 5823646283.2%

Reaction Steps

Aqueous potassium hydroxide (50% w/v, 1 ml) was added to a mixture of methyl 2-hydroxy-5-isopropyl-4-(methoxymethyloxy)benzoate (508 mg, 2.0 mmol) in methanol (10 ml) and water (4 ml) and the mixture was stirred and held at reflux for 6 hours. Upon cooling to room temperature the organic solvent was removed in vacuo and the residue acidified by the addition of 2M hydrochloric acid (30 ml). The solid material was collected by suction filtration, rinsed with water (2×20 ml) and sucked dry under reduced pressure to afford 2-hydroxy-5-isopropyl-4-(methoxymethyloxy)benzoic acid (400 mg, 83%) as a colourless solid. 1H NMR (DMSO-d6) 13.60 (1H, br s), 11.30 (1H, br s), 7.58 (1H, s), 6.58 (1H, s), 5.30 (2H, s), 3.42 (3H, s), 3.15 (1H, m), 1.18 (6H, d). MS: [M+H]+ 241.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08383619B2
Source datasetuspto-grants-2013_02
ORD IDord-2f0a64e505414ee39e477e1d7e9eae85
Source noteuspto-grants-2013_02