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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1850373Erstellt: 25. Oktober 2026

Hydrochloric Acid → 2-(2,3-Dimethylphenoxy)-2-methylpropanoic acid

https://huagongshe.com/reaction/1850373

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktHydrochloric AcidHCID 313—
Edukt2,3-DimethylphenolHCID 10687—
EduktSodium HydroxideHCID 14798—
Edukt2-Bromo-2-methylpropanoic acidHCID 74924—
LösungsmittelWaterHCID 962—
LösungsmittelDiethyl EtherHCID 3283—
LösungsmittelMethyl Ethyl KetoneHCID 6569—
Produkt2-(2,3-Dimethylphenoxy)-2-methylpropanoic acidHCID 153201345%

Reaktionsbedingungen

Temperatur50 °C

Reaktionsschritte

Sodium hydroxide (82.0 g, 2.05 mol) was added to a solution of methyl ethyl ketone (400 mL) containing 2,3-dimethylphenol (50.0 g, 410 mmol), and the mixture was stirred at 50° C. for 1 hour. After that, a solution of methyl ethyl ketone (200 mL) containing 2-bromo-2-methylpropionic acid (103 g, 615 mmol) was added thereto, and the mixture was stirred at 50° C. for 4 hours. After cooled to room temperature, the reaction solution was distributed by adding water and diethyl ether. 6N hydrochloric acid was added to the aqueous layer to be acidic, and then extraction was performed using ethyl acetate. The extract was washed with saturated saline, and then dried using anhydrous magnesium sulfate. The solvent was removed under reduced pressure, and the obtained residue was purified by silica gel chromatography (hexane-ethyl acetate 95:5 to 50/50) to give 38.3 g of the title compound (yield: 45%).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08957069B2
Quelldatensatzuspto-grants-2015_02
ORD IDord-bcdd452f0c374162b91c681230517bdd
Quellennotizuspto-grants-2015_02