HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 241815Generated: October 25, 2026
Potassium Hydroxide → 2,4-Bis(benzyloxy)-5-isopropenylbenzoic acid
https://huagongshe.com/reaction/241815
Participants
| Role | Name | HCID | Charge |
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| Reactant | Potassium Hydroxide | HCID 14797 | — |
| Reactant | Methyl 2,4-bis-benzyloxy-5-isopropenylbenzoate | HCID 11955870 | — |
| Solvent | Methanol | HCID 887 | — |
| Solvent | Water | HCID 962 | — |
| Product | 2,4-Bis(benzyloxy)-5-isopropenylbenzoic acid | HCID 49864016 | 100% |
Reaction Steps
Potassium hydroxide (10.96 g, 0.19 mmol) was added to a stirred suspension of methyl 2,4-bis-benzyloxy-5-isopropenyl-benzoate (61.0 g, 0.16 mol) in methanol (750 ml) and water (250 ml) and the mixture was stirred and held at reflux for 16 hours. Upon cooling the organic solvent was removed in vacuo and the mixture acidified to pH 2 or below by the addition of 2M hydrochloric acid (200 ml). The mixture was diluted with water (2 L) and extracted with ethyl acetate (2 L), the organic layer was separated and the solvent removed in vacuo to afford 2,4-bis-benzyloxy-5-isopropenyl-benzoic acid (58.8 g, 100%) as a colourless solid. 1H NMR (DMSO-d6) 7.52 (2H, d), 7.47-7.29 (9H, m), 6.82 (1H, s), 5.20 (2H, s), 5.17 (2H, s), 5.06 (1H, s), 5.04 (1H, s), 2.03 (3H, s). MS: [M+H]+ 375.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08653084B2 |
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| Source dataset | uspto-grants-2014_02 |
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| ORD ID | ord-7037689e225646a2ad5d6769d12b3138 |
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| Source note | uspto-grants-2014_02 |
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