HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2047295Generated: November 1, 2026
Lithium Hydroxide → 4-(2-Tert-butoxycarbonyl-ethyl)-3,5-dimethyl-benzoic acid
https://huagongshe.com/reaction/2047295
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Lithium Hydroxide | HCID 3939 | — |
| Reactant | 4-(2-Tert-butoxycarbonyl-ethyl)-3,5-dimethyl-benzoic acid methyl ester | HCID 66936173 | — |
| Solvent | Citric Acid | HCID 311 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | 4-(2-Tert-butoxycarbonyl-ethyl)-3,5-dimethyl-benzoic acid | HCID 59497932 | 49.4% |
Reaction Steps
To a solution of 4-(2-tert-butoxycarbonyl-ethyl)-3,5-dimethyl-benzoic acid methyl ester (10.8 g, 37.0 mmol) in ethanol (100 mL) a 2 M aq. solution of LiOH (50 mL) is added at 0° C. The turbid mixture is stirred at 0° C. for 30 min, then at rt for 4 h. The mixture is diluted with 10% aq. citric acid solution and extracted three times with diethyl ether. The combined org. extracts are dried over MgSO4, filtered and concentrated. The solid residue is suspended in diethyl ether/heptane, stirred at rt, and filtered. The slurry procedure in diethyl ether/heptane is repeated. The solid material is collected and dried under HV to give 4-(2-tert-butoxycarbonyl-ethyl)-3,5-dimethyl-benzoic acid (5.09 g) as a white crystalline powder; LC-MS: tR=0.95 min, [M+1]+=279.14; 1H NMR (CDCl3): δ 1.47 (s, 9H), 2.30-2.40 (m, 2H), 2.39 (s, 6H), 2.94-3.03 (m, 2H), 7.75 (s, 2H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08592460B2 |
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| Source dataset | uspto-grants-2013_11 |
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| ORD ID | ord-5ff4e50f9ac347fb94dc0a547f73e87c |
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| Source note | uspto-grants-2013_11 |
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