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
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Potassium Hydroxide | HCID 14797 | — |
| Reactant | Methyl 2-hydroxy-5-isopropyl-4-(methoxymethyloxy)benzoate | HCID 58236463 | — |
| Solvent | Methanol | HCID 887 | — |
| Solvent | Water | HCID 962 | — |
| Product | 2-Hydroxy-5-isopropyl-4-(methoxymethyloxy)benzoic acid | HCID 58236462 | 83.2% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US08383619B2 |
|---|
| Source dataset | uspto-grants-2013_02 |
|---|
| ORD ID | ord-2f0a64e505414ee39e477e1d7e9eae85 |
|---|
| Source note | uspto-grants-2013_02 |
|---|