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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 476733Generated: October 30, 2026

Cyclohexanol → HCID 14771304, compound

https://huagongshe.com/reaction/476733

Reaction equation

Participants

RoleNameHCIDCharge
ReactantCyclohexanolHCID 7966—
ReactantSodium hydrideHCID 24758—
Reactant1-Fluoro-2-nitrobenzeneHCID 73895—
Solvent1,4-DioxaneHCID 31275—
ProductHCID 14771304HCID 14771304—

Reaction Steps

To 40 ml of a dioxane suspension containing 0.92 g of 60% sodium hydride was added 2.5 ml of cyclohexanol at room temperature over a 15-minute period, and the mixture was stirred at the same temperature for 1 hour and then at 50° C. for 3.5 hours. The temperature of the reaction solution was returned to room temperature, 10 ml of a dioxane containing 3.2 g of 2-fluoronitrobenzene was added dropwise, and the mixture was stirred at room temperature overnight. The dioxane was evaporated, the residue was extracted with chloroform, and the chloroform layer was washed, in turn, with water and a saturated aqueous sodium chloride solution and then dried over anhydrous sodium sulfate. The solvent was evaporated to give an oil, which was then distilled under reduced pressure to give 3.8 g of 2-cyclohexyloxynitrobenzene.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04885367
Source datasetuspto-grants-1989_12
ORD IDord-86d185b0bfc440bdb9d5e1661b7cb626
Source noteuspto-grants-1989_12