HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2069398Generated: October 31, 2026
Potassium Permanganate → 4-Benzyloxy-3-ethyl-5-methyl-benzoic acid
https://huagongshe.com/reaction/2069398
Participants
| Role | Name | HCID | Charge |
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| Reactant | Potassium Permanganate | HCID 516875 | — |
| Reactant | 4-Benzyloxy-3-ethyl-5-methylbenzaldehyde | HCID 86639348 | — |
| Solvent | Acetone | HCID 180 | — |
| Product | 4-Benzyloxy-3-ethyl-5-methyl-benzoic acid | HCID 59497919 | 78% |
Reaction Steps
4-Benzyloxy-3-ethyl-5-methyl-benzaldehyde (1.4 g, 5.5 mmol) is dissolved in acetone (20 mL) and is slowly added to a cold solution of KMnO4 (1.74 g, 11 mmol) in 20% aq. acetone (25 mL). The reaction mixture is stirred at rt for 3 h, and then acetone is evaporated. The remaining aq. phase is acidified with 10% citric acid (60 mL) and is extracted with DCM (80 mL, 60 mL, 60 mL). The combined org. extracts are washed with brine, dried over MgSO4, filtered and evaporated. The crude product is purified by CC on silica gel eluting with heptane:EA (5:1 to 2:1) to give 4-benzyloxy-3-ethyl-5-methyl-benzoic acid (1.16 g) as an off-white solid; LC-MS: tR=0.56 min*; 1H NMR (CDCl3): δ 1.29 (t, J=7.5 Hz, 3H), 2.39 (s, 3H), 2.75 (q, J=7.5 Hz, 2H), 4.90 (s, 2H), 7.53-7.36 (m, 5H), 7.86 (s, 1H), 7.89 (s, 1H), 12.0 (s br, 1H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08299086B2 |
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| Source dataset | uspto-grants-2012_10 |
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| ORD ID | ord-2d73f23dec5744d08e0ef803385b142d |
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| Source note | uspto-grants-2012_10 |
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