HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2047306Generated: October 31, 2026
Hydrochloric Acid → 3-Ethyl-4-hydroxy-5-methyl-benzoic acid
https://huagongshe.com/reaction/2047306
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | 3-Ethyl-4-hydroxy-5-methylbenzaldehyde | HCID 23159210 | — |
| Reactant | Sodium Chlorite | HCID 23668197 | — |
| Solvent | Dimethyl Sulfoxide | HCID 679 | — |
| Solvent | Water | HCID 962 | — |
| Product | 3-Ethyl-4-hydroxy-5-methyl-benzoic acid | HCID 59234777 | 92.8% |
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 and 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
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US08592460B2 |
|---|
| Source dataset | uspto-grants-2013_11 |
|---|
| ORD ID | ord-e8b84bba69b3483b98da996a81f461dc |
|---|
| Source note | uspto-grants-2013_11 |
|---|