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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 436657Erstellt: 24. Oktober 2026

Potassium Iodide → 4-Cyclopropoxybenzoic acid

https://huagongshe.com/de/reaction/436657

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktPotassium IodideHCID 4875—
EduktEthylparabenHCID 8434—
EduktPotassium CarbonateHCID 11430—
EduktBromocyclopropaneHCID 78037—
EduktEthyl 4-(cyclopropyloxy)benzoateHCID 21453006—
LösungsmittelDimethylformamideHCID 6228—
Produkt4-Cyclopropoxybenzoic acidHCID 21452864—

Reaktionsschritte

The intermediate 4-cyclopropyloxybenzoic acid was prepared as follows: A 66.5 g. portion of ethyl 4-hydroxybenzoate was dissolved in 800 ml. of dimethylformamide and to the solution was added 83.0 g. of anhydrous potassium carbonate and 5 g. of potassium iodide. To the resulting stirred suspension was added 60.5 g. of cyclopropyl bromide. The stirred reaction mixture was refluxed for 6 days and the hot reaction mixture was filtered to remove the inorganic solids which were washed well with dimethylformamide. The combined filtrate and dimethylformamide washings were evaporated in vacuo and the remaining liquid-solid residue was taken up in a mixture of 500 ml. of water and 500 ml. of ether. The resulting mixture was shaken well and the layers were separated. The aqueous layer was extracted with 200 ml. of ether. The combined ether solutions were washed successively with two 250 ml. portions of aqueous potassium hydroxide solution, next with 200 ml. 0.5N hydrochloric acid and then with two 100 ml. portions of water. The ether solution was dried over anhydrous magnesium sulfate and the ether removed in vacuo to yield, as an amber liquid, 36.2 g. of ethyl 4-cyclopropyloxy-benzoate.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS04009208
Quelldatensatzuspto-grants-1977_02
ORD IDord-9958e0c525e74815a94420815c7b6e1b
Quellennotizuspto-grants-1977_02