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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 132716Erstellt: 26. Oktober 2026

Pyridine → 1,4-Bis(benzoyloxymethyl)cyclohexane

https://huagongshe.com/reaction/132716

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktPyridineHCID 1049—
EduktBenzoyl chlorideHCID 7412—
Edukt1,4-CyclohexanedimethanolHCID 7735—
EduktTetrahydrofuranHCID 8028—
Produkt1,4-Bis(benzoyloxymethyl)cyclohexaneHCID 11824495%

Reaktionsschritte

To 0.03 mol 1,4-dihydroxymethylcyclohexane were added 30 ml tetrahydrofuran and 0.09 mol pyridine, then added 0.075 mol benzoyl chloride with stirring. The reaction was heated refluxing for 4 hours, cooled and added 20 ml saturated saline. The reaction mixture was extracted with ethyl acetate, and the extract was dried over anhydrous sodium sulfate, filtered. After removing solvent, the crude was purified by recrystallization from ethyl acetate and petroleum ether (2:1 v/v) to give 1,4-di(benzoyloxymethyl)cyclohexane as a white solid. The yield was 95%, and m.p. was 111-113° C.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07388061B2
Quelldatensatzuspto-grants-2008_06
ORD IDord-b5d3024eff4646769e9da25fb1b1ae6a
Quellennotizuspto-grants-2008_06