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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2040801Generated: October 31, 2026

Hydrochloric Acid → 3-Ethyl-4-hydroxy-5-methyl-benzoic acid

https://huagongshe.com/reaction/2040801

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
Reactant3-Ethyl-4-hydroxy-5-methylbenzaldehydeHCID 23159210—
ReactantSodium ChloriteHCID 23668197—
SolventDimethyl SulfoxideHCID 679—
SolventWaterHCID 962—
Product3-Ethyl-4-hydroxy-5-methyl-benzoic acidHCID 5923477792.8%

Reaction Steps

To a solution of 3-ethyl-4-hydroxy-5-methyl-benzaldehyde (78.8 g, 0.48 mol) in DMSO (585 mL), a solution of NaH2PO4 dihydrate (17.3 g, 0.144 mol) in water (160 mL) is added over a period of 13 min. The mixture is stirred at rt an a solution of NaClO2 (65.17 g, 0.577 mol) in water (160 mL) is added while the mixture is cooled with an ice-bath. The mixture is stirred for 1 h before a second portion of NaClO2 (43.44 g, 0.480 mol) in water (100 mL) is added while the temperature is kept between 25 and 40° C. with an ice-bath. The yellow suspension is stirred at rt for 24 h before it is acidified with 32% aq. HCl to pH 2-3. The mixture is extracted with TBME (250 mL), the org. extract is washed with water, and the washings are extracted back with TBME. The solvent of the combined org. extracts is evaporated to give crude 3-ethyl-4-hydroxy-5-methyl-benzoic acid (80.3 g) as a yellow solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08580824B2
Source datasetuspto-grants-2013_11
ORD IDord-52628229b5dd4c4ca0ffa33a3d4bd4ce
Source noteuspto-grants-2013_11