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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 19235Erstellt: 24. Oktober 2026

2,5-Dichlorophenol → HCID 66894688, Verbindung

https://huagongshe.com/de/reaction/19235

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
Edukt2,5-DichlorophenolHCID 66—
Edukt3-Chloro-but-2-enoic acid ethyl esterHCID 282835—
EduktPotassium tert-butoxideHCID 23665647—
LösungsmittelTetrahydrofuranHCID 8028—
ProduktHCID 66894688HCID 6689468838%

Reaktionsbedingungen

Temperatur23 °C

Reaktionsschritte

Potassium t-butoxide (7.50 g, 0.067 mol) was added to a stirred solution of 2,5-dichloro-phenol (5.46 g, 0.033 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, 5.00 g, 0.034 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-(2,5-dichloro-phenoxy)-but-2-enoic acid ethyl ester (3.45 g, 37%) as a yellow oil.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07741327B2
Quelldatensatzuspto-grants-2010_06
ORD IDord-35c0f0d3fa224c79b5410e1cd99a7e4c
Quellennotizuspto-grants-2010_06