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HRID 56545Erstellt: 24. Oktober 2026

Potassium Hydroxide → 5-Bromo-2-(difluoromethoxy)-1,3-dimethoxybenzene

https://huagongshe.com/de/reaction/56545

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktPotassium HydroxideHCID 14797—
EduktBromodifluoromethyl diethylphosphonateHCID 144101—
Edukt4-Bromo-2,6-dimethoxyphenolHCID 14845876—
LösungsmittelWaterHCID 962—
LösungsmittelAcetonitrileHCID 6342—
Produkt5-Bromo-2-(difluoromethoxy)-1,3-dimethoxybenzeneHCID 5843207162%

Reaktionsbedingungen

Temperatur-78 °C

Reaktionsschritte

5-Bromo-2-(difluoromethoxy)-1,3-dimethoxybenzene was synthesized from 4-bromo-2,6-dimethoxyphenol according to the procedure of Zafrani, Y. Tetrahedron 2009, 65, 5278 as follows. To a solution of 4-bromo-2,6-dimethoxyphenol (1.08 g, 4.6 mmol) in MeCN (27 mL) was added a solution of KOH (5.0 g, 89 mmol) in H2O (27 mL). The mixture was immediately cooled over a −78° C. bath and diethyl(bromodifluoromethyl)phosphonate (1.6 mL, 8.9 mmol) was added. The flask was sealed with a septum and the cold bath was removed. The mixture was stirred for a total of 3.5 hrs during which time the septum was ejected from the flask. The reaction was diluted with EtOAc and the layers were separated. The aqueous layer was extracted with EtOAc and the combined organics were washed with 1 M NaOH, H2O and brine then dried over Na2SO4 and concentrated in vacuo. Purification by chromatography (0-30% EtOAc-hexanes) provided 5-bromo-2-(difluoromethoxy)-1,3-dimethoxybenzene as a white solid (0.808 g, 62% yield).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS09434707B2
Quelldatensatzuspto-grants-2016_09
ORD IDord-11df3402760d45b2a0c38bdeab5e3b2c
Quellennotizuspto-grants-2016_09