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HRID 347395Erstellt: 24. Oktober 2026

1,4-Dimethoxybenzene → 1-Acetoxy-2-methyl-3-(2,5-dimethoxyphenyl)propene

https://huagongshe.com/de/reaction/347395

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
Edukt1,4-DimethoxybenzeneHCID 9016—
EduktMethacrolein diacetateHCID 25305—
LösungsmittelEthyl AcetateHCID 8857—
Produkt1-Acetoxy-2-methyl-3-(2,5-dimethoxyphenyl)propeneHCID 6946538677,4%

Reaktionsbedingungen

Temperatur53.5 °C

Reaktionsschritte

In an argon gas atmosphere, a three necked flask having a capacity of 25 ml was charged with 1.92 g (10 m moles) of 3,3-diacetoxy-2-methylpropene having a purity degree of 89.6% by mass and 13.82 g (100 m moles) of hydroquinone dimethylether. Then, the resultant mixture was mixed with 0.14 g (1 m mole) of boron trifluoride-diethyl ether complex at an internal temperature of 54° C. over a time of one minute. The mixture was stirred at an internal temperature of 53 to 54° C. for one hour to cause the mixed compounds to react with each other. After the reaction was completed, the resultant reaction liquid was mixed with 150 ml of ethyl acetate and washed two times with 20 ml of saturated aqueous sodium chloride solution. The resultant reaction liquid was subjected to a layer separation treatment, the resultant organic layer was distilled under reduced pressure (20 mmHg, 55 to 57° C.), the resultant residue was refined by a chromatography on silica gel using an eluting solvent:hexane/ethyl acetate mixture in a mixing ratio by volume of 10/1. As a colorless liquid fraction, the target 1-acetoxy-2-methyl-3-(2,5-dimethoxyphenyl)propene was obtained in a yield of 77.4% in an amount of 1.94 g in the form of a colorless solid.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07173148B2
Quelldatensatzuspto-grants-2007_02
ORD IDord-c6025d56d0444595a1677ec7688d7cfa
Quellennotizuspto-grants-2007_02