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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2037345Generated: November 1, 2026

4-Benzyloxy-3-ethyl-5-methyl-benzoic acid tert-butyl ester → 3-Ethyl-4-hydroxy-5-methyl-benzoic acid tert-butyl ester

https://huagongshe.com/reaction/2037345

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-Benzyloxy-3-ethyl-5-methyl-benzoic acid tert-butyl esterHCID 66932009—
CatalystPalladiumHCID 23938—
SolventEthanolHCID 702—
SolventTetrahydrofuranHCID 8028—
Product3-Ethyl-4-hydroxy-5-methyl-benzoic acid tert-butyl esterHCID 66931984109.3%

Reaction Steps

To a solution of 4-benzyloxy-3-ethyl-5-methyl-benzoic acid tert.butyl ester (9.02 g, 27.6 mmol) in THF (50 mL) and ethanol (50 mL), Pd/C (400 mg, 10% Pd) is added. The slurry is stirred at rt for 24 h under 1 bar of H2. The catalyst is removed by filtration, the filtrate is concentrated, dissolved again in THF (50 mL) and ethanol (50 mL), and again treated with Pd/C (400 mg, 10% Pd). The slurry is stirred at rt for 24 h under 1 bar of H2. The catalyst is again removed by filtration and the filtrate is concentrated and dried to give 3-ethyl-4-hydroxy-5-methyl-benzoic acid tert.butyl ester (7.13 g) as a pale yellow oil; LC-MS: tR=1.01 min; 1H NMR (CDCl3): δ1.28 (t, J=7.8 Hz, 3H), 1.61 (s, 9H), 2.30 (s, 3H), 2.67 (q, J=7.5 Hz, 2H), 5.13 (s br, 1H), 7.67 (s, 1H), 7.69 (s, 1H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08575200B2
Source datasetuspto-grants-2013_11
ORD IDord-34db1294253f418daa22a8a3d48e3e8a
Source noteuspto-grants-2013_11