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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1743187Erstellt: 27. Oktober 2026

Water → (4-Isopropylphenyl)-2,2-dimethyl-2,3-dihydrobenzofuran-5-ol

https://huagongshe.com/reaction/1743187

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktWaterHCID 962—
EduktBenzene, 2-bromo-1,4-dimethoxy-HCID 91353—
Edukt2-(4-Isobutyrylphenyl)propaneHCID 4251244—
EduktButyllithiumHCID 178418339—
LösungsmittelTetrahydrofuranHCID 8028—
Produkt(4-Isopropylphenyl)-2,2-dimethyl-2,3-dihydrobenzofuran-5-olHCID 2223826370%

Reaktionsschritte

n-Butyllithium (1.6 M, 20.8 mL, 33.2 mmol) was added to a solution of 1-bromo-2,5-dimethoxybenzene (7.2 g, 33.2 mmol) in tetrahydrofuran (20 mL) at −78° C., and the mixture was stirred for 20 minutes at the same temperature. To the reaction mixture was added 1-(4-isopropylphenyl)-2-methylpropan-1-one (5.70 g, 30.0 mmol), and the mixture was stirred for 30 minutes at room temperature. Water (30 mL) was poured into the reaction mixture, which was then extracted three times with ethyl acetate. The organic layers were combined, washed with water, dried over magnesium sulfate, filtered, and concentrated under reduced pressure. A mixture of the residue and 48% hydrobromic acid (30 mL) was heated under reflux for 24 hours in an argon atmosphere. After cooling, water (30 mL) was added to the reaction mixture, which was then extracted twice with ethyl acetate. The organic layers were combined, washed with water, dried over magnesium sulfate, filtered, and concentrated under reduced pressure. The residue was crystallized from isopropyl ether-hexane to obtain the title compound (2.1 g, yield 70%).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07008950B1
Quelldatensatzuspto-grants-2006_03
ORD IDord-bf47bb5b6d2240ef8c3bbc18a2523bd7
Quellennotizuspto-grants-2006_03