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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 132716Generated: October 26, 2026

Pyridine → 1,4-Bis(benzoyloxymethyl)cyclohexane

https://huagongshe.com/reaction/132716

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPyridineHCID 1049—
ReactantBenzoyl chlorideHCID 7412—
Reactant1,4-CyclohexanedimethanolHCID 7735—
ReactantTetrahydrofuranHCID 8028—
Product1,4-Bis(benzoyloxymethyl)cyclohexaneHCID 11824495%

Reaction Steps

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.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07388061B2
Source datasetuspto-grants-2008_06
ORD IDord-b5d3024eff4646769e9da25fb1b1ae6a
Source noteuspto-grants-2008_06