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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 541371Generated: October 30, 2026

Methyl chloroformate → 4-Cyclopropyl-2-ethyl-5-(methoxycarbonyl)benzoic acid

https://huagongshe.com/reaction/541371

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethyl chloroformateHCID 6586—
Reactant4-Cyclopropyl-2-ethyl-5-iodobenzoic acidHCID 68288927—
ReactantButyllithiumHCID 178418339—
SolventEther tetrahydrofuranHCID 21868444—
Product4-Cyclopropyl-2-ethyl-5-(methoxycarbonyl)benzoic acidHCID 68288152102%

Reaction Conditions

Temperature-78 °C

Reaction Steps

To a solution of 4-cyclopropyl-2-ethyl-5-iodobenzoic acid (compound 226.5, 500 mg, 1.58 mmol, 1.00 equiv) in THF/Et2O (10/10 mL) under nitrogen at −78° C. was added dropwise n-butyllithium (2.5 M, 1.88 mL, 3.00 equiv) over 3 min. After stirring for 10 min at −78° C., methyl chloroformate (230 mg, 2.43 mmol, 1.50 equiv) was added dropwise at −78° C. The resulting solution was stirred for 40 min at −78° C., then warmed slowly to −35° C. The reaction was carefully quenched with 2 mL of water. The pH was adjusted to ˜4-5 with hydrogen chloride (aq., 1 M). The resulting mixture was extracted with 3×20 mL of ethyl acetate and the combined organic layers were dried (Na2SO4) and concentrated under reduced pressure to yield 400 mg the title compound as a yellow solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08871790B2
Source datasetuspto-grants-2014_10
ORD IDord-747570201f1e4814bc98ef12ae9968ee
Source noteuspto-grants-2014_10