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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 460310Erstellt: 25. Oktober 2026

Water → 4-Bromo-6-isobutyl-benzo[1,3]dioxole

https://huagongshe.com/reaction/460310

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktWaterHCID 962—
EduktTrifluoroacetic acidHCID 6422—
EduktTriethylsilaneHCID 12052—
Edukt1-(7-Bromo-benzo[1,3]dioxol-5-yl)-2-methyl-propan-1-olHCID 18445394—
LösungsmittelDichloromethaneHCID 6344—
Produkt4-Bromo-6-isobutyl-benzo[1,3]dioxoleHCID 1844541552%

Reaktionsbedingungen

Temperatur0 °C

Reaktionsschritte

To a cold solution (0° C.) of 1-(7-bromo-benzo[1,3]dioxol-5-yl)-2-methyl-propan-1-ol (498 mg, 1.82 mmol) in dry dichloromethane (10 mL) was added triethylsilane (0.6 mL, 3.65 mmol). After 15 minutes, trifluoroacetic acid was added to the reaction and the mixture stirred at 0° C. for 45 minutes. Water was poured into the reaction mixture and the layers separated. The organic layer was further washed with water, aqueous NaHCO3 and brine, dried (MgSO4), filtered and evaporated. The residue was purified on silica gel (5% ethyl acetate in hexane) to give 242 mg of 4-bromo-6-isobutyl-benzo[1,3]dioxole (52%). 1H NMR (300 MHz; CDCl3): δ 0.90 (d, J=6.3 Hz, 6H), 1.81 (m, 1H), 2.39 (d, J=7.5 Hz, 2H), 6.01 (s, 2H), 6.58 (s, 1H), 6.76 (s, 1H).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07196108B2
Quelldatensatzuspto-grants-2007_03
ORD IDord-6fcf7cb8bdb94600a5a6b80f990952fd
Quellennotizuspto-grants-2007_03