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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 541346Generated: October 31, 2026

Dimethyl Carbonate → 4-Cyclobutyl-2-ethyl-5-(methoxycarbonyl)benzoic acid

https://huagongshe.com/reaction/541346

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDimethyl CarbonateHCID 12021—
Reactant4-Cyclobutyl-2-ethyl-5-iodobenzoic acidHCID 68288909—
ReactantButyllithiumHCID 178418339—
SolventTetrahydrofuranHCID 8028—
Product4-Cyclobutyl-2-ethyl-5-(methoxycarbonyl)benzoic acidHCID 6828893369%

Reaction Conditions

Temperature25 °C

Reaction Steps

To a solution of 4-cyclobutyl-2-ethyl-5-iodobenzoic acid (compound 215.3, 3.30 g, 10.0 mmol, 1.00 equiv) in THF (40 mL) was added n-BuLi (2.5 M, 9.50 mL, 2.38 equiv) dropwise at −78° C. under nitrogen atmosphere. The resulting solution was stirred for another 20 min at the same temperature, followed by the addition of a solution of dimethyl carbonate (2.70 g, 30.0 mmol, 3.00 equiv) in tetrahydrofuran (2 mL) dropwise. The reaction temperature was slowly raised to 25° C. and stirred for another 1 h, then slowly quenched with 50 mL of water. The pH was adjusted to ˜4 with HCl (aq., 1 M) and the resulting mixture was extracted with 100 mL of ethyl acetate. The combined organic layers were dried over anhydrous sodium sulfate and concentrated in vacuo. The residue was purified by silica gel chromatography with ethyl acetate/petroleum ether (1:3) as eluent to furnish 1.80 g (69%) of the desired product as a white solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08871790B2
Source datasetuspto-grants-2014_10
ORD IDord-ca11862a47934f618e979e7dca5691f4
Source noteuspto-grants-2014_10