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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1527962Erstellt: 25. Oktober 2026

Acetic Acid → 3-(4-Bromophenyl)-3-o-tolylpropanoic acid

https://huagongshe.com/reaction/1527962

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktAcetic AcidHCID 176—
EduktSulfuric AcidHCID 1118—
EduktEthyl 3-(4-bromophenyl)-2-cyano-3-o-tolylpropanoateHCID 67015643—
LösungsmittelEthyl AcetateHCID 8857—
Produkt3-(4-Bromophenyl)-3-o-tolylpropanoic acidHCID 6701562221,9%

Reaktionsschritte

Sulfuric acid (940 g, 9.59 mol) was added over 30 min under ice cooling to a mixture of ethyl 3-(4-bromophenyl)-2-cyano-3-o-tolylpropanoate (200 g, 494 mmol) in acetic acid (1.06 kg, 17.7 mol), while keeping the internal temperature below 27° C., then the reaction mixture was heated at reflux for 20 h. After cooling to 40° C. ice (500 g) and ethyl acetate (1500 mL) were added, the precipitate collected by filtration and washed with water to produce the title compound (34.5 g). The filtrate was partitioned between ethyl acetate and water, the organic layer was washed with brine, dried over magnesium sulfate, filtered, and evaporated. The residue was stored in the refrigerator for 1 h. Then the precipitate was collected by filtration and washed with acetic acid and heptane to afford a second crop of product (96.2 g). Total yield: 130.7 g (83%). Off-white solid, MS: 319.0 [M−H]−.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS09090565B2
Quelldatensatzuspto-grants-2015_07
ORD IDord-6e7de0c5112c4c35bf703cf39c82d7bd
Quellennotizuspto-grants-2015_07