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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 19279Erstellt: 24. Oktober 2026

M-Cresol → (E)-3-m-tolyloxy-but-2-enoic acid ethyl ester

https://huagongshe.com/de/reaction/19279

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktM-CresolHCID 342—
Edukt3-Chloro-but-2-enoic acid ethyl esterHCID 282835—
EduktPotassium tert-butoxideHCID 23665647—
LösungsmittelTetrahydrofuranHCID 8028—
Produkt(E)-3-m-tolyloxy-but-2-enoic acid ethyl esterHCID 1224119763,3%

Reaktionsbedingungen

Temperatur23 °C

Reaktionsschritte

Potassium t-butoxide (10.4 g, 0.092 mol) was added to a stirred solution of 3-methyl-phenol (5.00 g, 0.046 mol) in tetrahydrofuran (35 mL) at 23° C. under nitrogen and the reaction mixture was heated to reflux for 0.75 h. The reaction mixture was cooled to 23° C. and a solution of 3-chloro-but-2-enoic acid ethyl ester (prepared as in Example 191, 6.85 g, 0.046 mol) in tetrahydrofuran (40 mL) was added to the reaction mixture. The reaction mixture was refluxed for an additional 3 h. After this time, the mixture was concentrated in vacuo and the residue was diluted with water and extracted with diethyl ether. The organic layer was then washed with 5% aqueous sodium hydroxide solution followed by a saturated aqueous sodium chloride solution, dried over sodium sulfate and concentrated in vacuo to afford (E)-3-m-tolyloxy-but-2-enoic acid ethyl ester (6.41 g, 63%) as a yellow oil.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07741327B2
Quelldatensatzuspto-grants-2010_06
ORD IDord-933c811e9bc548a696a80249e8acda47
Quellennotizuspto-grants-2010_06