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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1718955Generated: October 26, 2026

Pyridine → 4-Hydroxycyclohexyl benzoate

https://huagongshe.com/reaction/1718955

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPyridineHCID 1049—
ReactantBenzoyl chlorideHCID 7412—
ReactantTetrahydrofuranHCID 8028—
ReactantCyclohexane-1,1-diolHCID 19352763—
Product4-Hydroxycyclohexyl benzoateHCID 23810986%

Reaction Steps

A mixture of benzoyl chloride (50 mL), cyclohexanediol (150 g), pyridine (105 mL) and tetrahydrofuran (1300 mL) was stirred at room temperature overnight. The reaction mixture was concentrated under reduced pressure, the residue was diluted with ethyl acetate, successively washed with saturated aqueous sodium hydrogen carbonate, water, and brine, dried over anhydrous magnesium sulfate, and concentrated under reduced pressure. The residue was purified by silica gel column chromatography to give the title compound as a colorless oil (81.5 g, 86%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07803940B2
Source datasetuspto-grants-2010_09
ORD IDord-29f4e48b7ce14b9c9b02d5bb20cce98f
Source noteuspto-grants-2010_09