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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 255937Generated: October 31, 2026

Potassium Carbonate → 1-(2,3-Dichloro-4-butyrylphenoxy)cyclobutane-1-carboxylic acid

https://huagongshe.com/reaction/255937

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium CarbonateHCID 11430—
ReactantEthyl 1-bromocyclobutanecarboxylateHCID 97595—
Reactant1-(2,3-Dichloro-4-hydroxyphenyl)butan-1-oneHCID 14099856—
SolventDimethylformamideHCID 6228—
Product1-(2,3-Dichloro-4-butyrylphenoxy)cyclobutane-1-carboxylic acidHCID 20148698—

Reaction Conditions

Temperature65 °C

Reaction Steps

A mixture of 2,3-dichloro-4-butyrylphenol (7 g, 0.03 mole), ethyl 1-bromocyclobutanecarboxylate (10.23 g, 0.049 mole) and potassium carbonate (7.5 g, 0.054 mole) in N,N-dimethylformamide (60 ml) was stirred and heated at 65° C. for 18 hours. The reaction mixture was poured into ice water and the resulting mixture was extracted with ether. The ether extract was washed with a 1% sodium hydroxide solution, then with water and finally dried over MgSO4. The ether was evaporated in vacuo and the residue treated with acetic acid (60 ml) and 5% hydrochloric acid (15 ml). The mixture was stirred and refluxed overnight. The solvents were evaporated in vacuo. The residue was chromatographed over a column containing silica gel (140 g) using methylene chloride/tetrahydrofuran/acetic acid 50/1/1 as the eluent. The pertinent fractions were united, treated with toluene and evaporated in vacuo to obtain 1-(2,3-dichloro-4-butyrylphenoxy)cyclobutane-1-carboxylic acid as a liquid whose identity was confirmed by NMR and purity by thin layer chromatography.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04699926
Source datasetuspto-grants-1987_10
ORD IDord-73cd8f7c18c04b6f96cb517683a466ec
Source noteuspto-grants-1987_10