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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

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium PermanganateHCID 516875—
Reactant4-Benzyloxy-3-ethyl-5-methylbenzaldehydeHCID 86639348—
SolventAcetoneHCID 180—
Product4-Benzyloxy-3-ethyl-5-methyl-benzoic acidHCID 5949791978%

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08299086B2
Source datasetuspto-grants-2012_10
ORD IDord-2d73f23dec5744d08e0ef803385b142d
Source noteuspto-grants-2012_10