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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1656705Erstellt: 24. Oktober 2026

Water → Methyl alpha-(2-methoxymethylphenyl)-beta-methylacrylate

https://huagongshe.com/de/reaction/1656705

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktWaterHCID 962—
EduktMethyl 2-methoxymethylphenylglyoxylateHCID 19937173—
EduktPotassium tert-butoxideHCID 23665647—
KatalysatorPhosphonium, ethyltriphenyl-, bromide (1:1)HCID 73727—
LösungsmittelTetrahydrofuranHCID 8028—
ProduktMethyl alpha-(2-methoxymethylphenyl)-beta-methylacrylateHCID 5426868978,1%

Reaktionsbedingungen

Temperatur5 °C

Reaktionsschritte

37.1 g (100 mmol) of ethyltriphenylphosphonium bromide are introduced under nitrogen into 300 ml of absolute tetrahydrofuran. At 5° C., 11.2 g (0.1 mol) of potassium t-butanolate are added. After stirring at 5° C. for one hour, 20.8 g (100 mmol) of methyl 2-methoxymethylphenylglyoxylate in 100 ml of tetrahydrofuran are added dropwise. The mixture is stirred at 5° C. for one hour and at 25° C. for one hour, 200 ml of water are added, the mixture is extracted with methylene chloride and the organic phases are washed with water. After drying over sodium sulfate, the solvent is removed under reduced pressure. The residue is purified by chromatography on a silica gel column (methyl tert-butyl ether/n-hexane=1/2). 17.2 g (78%) of the abovementioned ester are obtained as an oil (Z/E isomer=1/9).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS05254717
Quelldatensatzuspto-grants-1993_10
ORD IDord-430c73b53cba4c019b60cda228d80024
Quellennotizuspto-grants-1993_10