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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1676121Generated: October 30, 2026

Lithium Hydroxide → 4-(2-Tert-butoxycarbonyl-ethyl)-3,5-dimethyl-benzoic acid

https://huagongshe.com/reaction/1676121

Reaction equation

Participants

RoleNameHCIDCharge
ReactantLithium HydroxideHCID 3939—
Reactant4-(2-Tert-butoxycarbonyl-ethyl)-3,5-dimethyl-benzoic acid methyl esterHCID 66936173—
SolventCitric AcidHCID 311—
SolventEthanolHCID 702—
Product4-(2-Tert-butoxycarbonyl-ethyl)-3,5-dimethyl-benzoic acidHCID 5949793249.4%

Reaction Conditions

Temperature0 °C

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 organic 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, 9 H), 2.30-2.40 (m, 2 H), 2.39 (s, 6 H), 2.94-3.03 (m, 2 H), 7.75 (s, 2 H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08003800B2
Source datasetuspto-grants-2011_08
ORD IDord-003f94326edf4134b5e15827d22d4649
Source noteuspto-grants-2011_08