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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1646622Generated: November 1, 2026

Water → HCID 10039345, compound

https://huagongshe.com/reaction/1646622

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantMorpholineHCID 8083—
ReactantCycloheptanoneHCID 10400—
Reactant2-Bromobenzyl bromideHCID 76965—
Catalystp-Toluenesulfonic acidHCID 6101—
SolventTolueneHCID 1140—
Solvent1,4-DioxaneHCID 31275—
ProductHCID 10039345HCID 1003934555%

Reaction Steps

To a solution of cycloheptanone (56.1 g, 0.5 mol) in toluene (500 ml) was added morpholine (65.3 g, 0.75 mol) and tosic acid (100 mg). The reaction vessel was fitted with a Dean-Stark condenser and the reaction was refluxed for 24 hours. The toluene was removed in vacuo and the enamine was vacuum distilled. The enamine was collected as a pale yellow oil (46.5 g, 51%). To a solution of the enamine (10.0 g, 0.055 mol) in dioxane (50 ml) was added 2-bromobenzyl bromide and the reaction was refluxed overnight. Water (10 ml) was then added and the mixture was refluxed an additional 2 hours. The reaction was cooled and the solvent was removed in vacuo. The residue was partitioned between dichloromethane and 1N hydrochloric acid. The dichloromethane layer was washed with additional 1N hydrochloric acid (50 ml) and water (50 ml), dried (MgSO4), filtered, and reduced in volume to yield a crude orange oil (15.9 g). The mixture was vacuum distilled to yield the title compound as a clear oil (8.5 g, 55%) that was a semisolid at 23° C. ##STR91##

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05180736
Source datasetuspto-grants-1993_01
ORD IDord-989c660ae00b48928d8e77bce8b17b69
Source noteuspto-grants-1993_01