HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1881796Generated: November 2, 2026
Hydrochloric Acid → 2-Methoxy-4-methylbenzoic acid
https://huagongshe.com/reaction/1881796
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | 2-Hydroxy-p-toluic acid | HCID 5788 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | Potassium Hydroxide | HCID 14797 | — |
| Catalyst | Methyl iodide | HCID 6328 | — |
| Solvent | Acetone | HCID 180 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | 2-Methoxy-4-methylbenzoic acid | HCID 597164 | 24,462.6% |
Reaction Steps
To a solution of 2-hydroxy-4-methylbenzoic acid (25 g, 0.164 mol) in acetone (350 mL) was added K2CO3 (68 g, 0.492 mmol) followed by MeI (41 mL, 0.656 mmol) and the reaction mixture heated at reflux for 48 hrs. After cooling to r.t. the reaction mixture was filtered and the filtrate was evaporated to give the crude methyl 2-methoxy-4-methylbenzoate. KOH (11.3 g, 1.2 eq) was dissolved in MeOH (300 mL) and the crude ester was added to the mixture and the solution heated at reflux 48 hrs. After cooling the reaction mixture was acidified with aq. HCl (1N) and extracted with ethyl acetate. The organic layer was washed with brine, dried over MgSO4, filtered and evaporated. The residue was triturated with Ethyl acetate/Hexane to give 20 g of 2-methoxy-4-methylbenzoic acid as a cream white solid (85% yield)
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US08318947B2 |
|---|
| Source dataset | uspto-grants-2012_11 |
|---|
| ORD ID | ord-e23ccd826c9f48e19f6b63a957f0b187 |
|---|
| Source note | uspto-grants-2012_11 |
|---|