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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 232375Erstellt: 25. Oktober 2026

Potassium Hydroxide → HCID 20059753, Verbindung

https://huagongshe.com/reaction/232375

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktPotassium HydroxideHCID 14797—
Edukt2,4-DichlorobenzenethiolHCID 70730—
EduktEthyl 2-bromopropionateHCID 79040—
LösungsmittelAcetoneHCID 180—
ProduktHCID 20059753HCID 2005975325%

Reaktionsschritte

A mixture of 11.78 g of 2,4-dichlorothiophenol and 12.0 g of potassium hydroxide in 50 ml of acetone was stirred and heated to reflux. 11.77 g of ethyl 2-bromopropionate were added gradually and the mixture was heated under reflux for 22 hours. After cooling to room temperature, the mixture was filtered and the filtrate was evaporated to dryness. The residue was taken up in 400 ml of diethyl ether and the solution was washed with 400 ml of water and 400 ml of 10% sodium carbonate solution, dried over anhydrous sodium sulfate and evaporated to dryness. A solution of the residue in a mixture of 30 ml of ethanol and 17 ml of 10% potassium hydroxide solution was heated under reflux for 21 hours. The solution was evaporated to dryness and the residue was dissolved in 50 ml of water. The resulting solution was washed twice with 50 ml of diethyl ether each time and then acidified with concentrated hydrochloric acid and extracted twice with 150 ml of ethyl acetate each time. The combined organic extracts were washed twice with 200 ml of water each time, dried over anhydrous sodium sulfate and evaporated to dryness. The residue was recrystallized from diethyl ether to give 4.08 g of 2(RS)-(2,4-dichlorophenyl-thio)propionic acid in the form of a yellow solid of melting point 95°-98° C.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS04851519
Quelldatensatzuspto-grants-1989_07
ORD IDord-11d0318cb17b4ada8941a19dd8dac165
Quellennotizuspto-grants-1989_07