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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1835754Generated: October 30, 2026

Cyclohexanone → HCID 11084070, compound

https://huagongshe.com/reaction/1835754

Reaction equation

Participants

RoleNameHCIDCharge
ReactantCyclohexanoneHCID 7967—
ReactantEthyl AcetateHCID 8857—
ReactantHomoallyl bromideHCID 21241—
ReactantPotassium tert-butoxideHCID 23665647—
SolventTolueneHCID 1140—
ProductHCID 11084070HCID 11084070—

Reaction Conditions

Temperature0 °C

Reaction Steps

Ex-18a) A suspension of potassium t-butoxide in toluene cooled to 0° C. in an ice bath under N2 is treated with cyclohexanone. To the reaction mixture is slowly added 3-butenyl bromide. The reaction is warmed to room temperature. The reaction is then poured into EtOAc and washed once with 10% potassium hydrogen sulfate. The organic solution is then washed with brine, dried over magnesium sulfate, and the solvent evaporated under reduced pressure to afford 2-(3-butenyl) cyclohexanone.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06774126B2
Source datasetuspto-grants-2004_08
ORD IDord-2821b8840ce348a6ad0203d5f827e5da
Source noteuspto-grants-2004_08