Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1275032Generated: November 4, 2026

Cyclohexene oxide → HCID 12043059, compound

https://huagongshe.com/reaction/1275032

Reaction equation

Participants

RoleNameHCIDCharge
ReactantCyclohexene oxideHCID 9246—
Reactant1,2,3-TrimethoxybenzeneHCID 12462—
Reactant4-MethoxybenzaldehydeHCID 31244—
ReactantAluminum(III) ChlorideHCID 6451240—
SolventWaterHCID 962—
SolventDichloromethaneHCID 6344—
ProductHCID 12043059HCID 12043059—

Reaction Conditions

Temperature-78 °C

Reaction Steps

Cyclohexene oxide (90.2 ml; 0.89 mol) was added dropwise to a mechanically stirred mixture of trimethoxybenzene (I, 100 g; 0.594 mol) and aluminum chloride (118.82 g; 0.89 mol) in dichloromethane (500 ml) cooled at -78° C. The addition was done over a period of 50 min. The reaction mixture was allowed to stir at that temperature and the progress of the reaction monitored by TLC (tlc system 25% ethyl acetate-pet ether; anisaldehyde spray; pdt. Rf-value 0.35). The reaction mixture was worked up after 3 hours by adding cold-water (400 ml) and extracting with ethyl acetate (4×400 ml). The combined organic layers were washed with water, brine, and dried over sodium sulphate. The solvents were removed in-vacuo at a rotary evaporator. The oily residue was crystallized from pet ether (400 ml) to get the crystals of the title compound (62 g). The mother liquor, on evaporation of the solvents followed by chromatography over silica gel (column diam. 9.5 cm; silica gel 800 g; eluent 10, 25 and 40% ethyl acetate-pet ether), gave 28 g of the title compound. In total, 90 g (yield 57%; mp. 125-27° C.) of the title compound was isolated.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06159988
Source datasetuspto-grants-2000_12
ORD IDord-02fc833c56e64df1b62e0c7162adeceb
Source noteuspto-grants-2000_12