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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 347611Erstellt: 25. Oktober 2026

Phthalic Acid → 2-(5-Bromo-2,4-dihydroxybenzoyl)benzoic acid

https://huagongshe.com/reaction/347611

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktPhthalic AcidHCID 1017—
EduktPhthalic AnhydrideHCID 6811—
Edukt4-BromoresorcinolHCID 81105—
EduktAluminum(III) ChlorideHCID 6451240—
LösungsmittelDichloromethaneHCID 6344—
LösungsmittelNitromethaneHCID 6375—
LösungsmittelEthyl AcetateHCID 8857—
Lösungsmittel1,1,1,2-TetrachloroethaneHCID 12418—
Produkt2-(5-Bromo-2,4-dihydroxybenzoyl)benzoic acidHCID 22315707—

Reaktionsschritte

Aluminum chloride (8.48 g, 64 mmol) was added to a stirring suspension of phthalic anhydride (2.36 g, 16 mmol) in tetrachloroethane (40 mL) under nitrogen. Nitromethane (6 mL) was added to dissolve the reactants. 4-Bromoresorcinol (3 g, 16 mmol) was added and the mixture continued to stir under nitrogen. The reaction was monitored by high performance liquid chromatography (HPLC) over a period of 2 hours. It was observed that the reaction had ceased within the first 30 minutes, with starting materials remaining. The solution was diluted with ethyl acetate (˜150 mL) and washed with 1M hydrochloric acid (2×100 mL). The product was extracted from the organic layer into a saturated solution of sodium bicarbonate in water (200 mL). The basic aqueous phase was acidified with 3M hydrochloric acid to a pH of 5. The product was extracted from the aqueous phase into ethyl acetate (150 mL), washed with brine (2×100 mL), dried over magnesium sulfate and concentrated to give an orange oil which solidified upon standing for about 10 minutes. The solid was slurried in dichloromethane (20 mL) and filtered to give a mixture of the desired product and phthalic acid. Slurrying in water (20 mL) followed by filtration gave the desired product as a beige powder (1.72 g, 5.1 mmol, 32% yield).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07176161B2
Quelldatensatzuspto-grants-2007_02
ORD IDord-3aa5dd1eefb84480ae8bbc31e49694dd
Quellennotizuspto-grants-2007_02