Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 849149Generated: October 30, 2026

Cyclohexanone → 2-(2-Methoxyethyl)cyclohexanone

https://huagongshe.com/reaction/849149

Reaction equation

Participants

RoleNameHCIDCharge
ReactantCyclohexanoneHCID 7967—
Reactant2-Bromoethyl methyl etherHCID 80972—
ReactantPotassium tert-butoxideHCID 23665647—
SolventBenzeneHCID 241—
SolventWaterHCID 962—
SolventDiethyl EtherHCID 3283—
SolventPotassium bisulfateHCID 516920—
Product2-(2-Methoxyethyl)cyclohexanoneHCID 56663135%

Reaction Conditions

Temperature0 °C

Reaction Steps

Example 241 A) To a mechanically stirred mixture of KOt-Bu (87 g, 0.9 mol) in benzene (700 mL) cooled to 0° C. under an N2 atmosphere was added cyclohexanone (67 g, 0.75 mol) dropwise over 15 minutes. Ten minutes after the addition was complete, bromoethyl methylether (90 g, 0.78 mol) was added dropwise over 20 minutes. The reaction mixture was warmed to room temperature, refluxed for 7 hours, stirred at room temperature for 18 hours, and diluted with 0.5N potassium hydrogen sulfate (300 mL). The mixture was further diluted with Et2O (600 mL), 0.5N potassium hydrogen sulfate (200 mL), and water (200 mL) before the organic phase was separated. The organic layer was washed with water (200 mL) and brine (200 mL), dried (Na2SO4), filtered, and concentrated under reduced pressure. The crude product was distilled to afford 41 g (25% yield) of 2-(2-methoxyethyl)cyclohexanone.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06011028
Source datasetuspto-grants-2000_01
ORD IDord-85c8193d521d4289bff90074b549c7d0
Source noteuspto-grants-2000_01