HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 389959Generated: October 30, 2026
Potassium Hydroxide → 2-Allyloxy-4-hydroxy-5-isopropylbenzoic acid
https://huagongshe.com/reaction/389959
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Potassium Hydroxide | HCID 14797 | — |
| Reactant | Methyl 2-allyloxy-4-hydroxy-5-isopropylbenzoate | HCID 58236453 | — |
| Solvent | Methanol | HCID 887 | — |
| Solvent | Water | HCID 962 | — |
| Product | 2-Allyloxy-4-hydroxy-5-isopropylbenzoic acid | HCID 58236456 | 88% |
Reaction Steps
Aqueous potassium hydroxide (50% w/v, 2 ml) was added to a mixture of methyl 2-allyloxy-4-hydroxy-5-isopropylbenzoate (860 mg, 3.44 mmol) in methanol (12 ml) and water (4 ml) and the mixture was stirred and held at reflux for 5 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-allyloxy-4-hydroxy-5-isopropylbenzoic acid (715 mg, 88%) as a pale green solid. 1H NMR (DMSO-d6) 11.92 (1H, br s), 10.08 (1H, s), 7.56 (1H, s), 6.48 (1H, s), 6.03 (1H, m), 5.50 (1H, dm), 5.27 (1H, dm), 4.53 (2H, m), 3.11 (1H, m), 1.13 (6H, d). MS: [M+Na]+ 259.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08383619B2 |
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| Source dataset | uspto-grants-2013_02 |
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| ORD ID | ord-84a82ca80f4c4fad940e65be0114fd63 |
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| Source note | uspto-grants-2013_02 |
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