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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 541378Generated: October 27, 2026

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

https://huagongshe.com/reaction/541378

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDimethyl CarbonateHCID 12021—
Reactant4-Cyclobutyl-5-iodo-2-methylbenzoic acidHCID 68288671—
ReactantButyllithiumHCID 178418339—
SolventTetrahydrofuranHCID 8028—
Product4-Cyclobutyl-5-(methoxycarbonyl)-2-methylbenzoic acidHCID 6828833655.2%

Reaction Conditions

Temperature-78 °C

Reaction Steps

To a solution of 4-cyclobutyl-5-iodo-2-methylbenzoic acid (compound 230.1, 3.00 g, 9.49 mmol, 1.00 equiv) in THF (40 mL) under nitrogen at −78° C. was added dropwise n-BuLi (9.5 mL, 2.50 equiv, 2.5 M in THF). After 10 minutes, a solution of dimethyl carbonate (2.56 g, 28.4 mmol, 3.00 equiv) in THF (10 mL) was added dropwise at −78° C. The resulting solution was stirred for 1 h at −78° C., then carefully quenched by slow addition of 50 mL of water. The pH was adjusted to ˜4 with hydrogen chloride (aq., 1 M). The resulting mixture was extracted with 2×80 mL of ethyl acetate, the combined organic layers were dried over anhydrous sodium sulfate and concentrated in vacuo. The residue was purified using silica gel column chromatography with ethyl acetate/petroleum ether (1:10-1:2) as eluent to furnish 1.30 g (55%) of 4-cyclobutyl-5-(methoxycarbonyl)-2-methylbenzoic acid as a white solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08871790B2
Source datasetuspto-grants-2014_10
ORD IDord-ded5398d703d4137b5aa051601d9354b
Source noteuspto-grants-2014_10