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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 343473Erstellt: 24. Oktober 2026

Triisopropyl borate → 4-Ethoxyphenylboronic acid

https://huagongshe.com/de/reaction/343473

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktTriisopropyl borateHCID 21531—
Edukt4-BromophenetoleHCID 68523—
EduktMagnesiumHCID 5462224—
LösungsmittelTetrahydrofuranHCID 8028—
Produkt4-Ethoxyphenylboronic acidHCID 273435167,4%

Reaktionsschritte

A one-necked, 25-mL, round-bottomed flask equipped with a reflux condenser fitted with an argon inlet adapter was charged with magnesium powder (0.255 g, 10.5 mmol, -50 mesh), 7 mL THF, and 4-bromophenetol (1.41 g, 1.00 mL, 7.00 mmol). The resulting mixture was heated to reflux for 3 h. A second one-necked, 25-mL, round- bottomed flask equipped with a rubber septum and an argon inlet needle was charged with triisopropyl borate (3.95 g, 4.85 mL, 21.00 mmol) and cooled to -78° C. while the Grignard reagent prepared above was added dropwise via cannula over ca. 5 min. The cooling bath was removed and the reaction mixture was stirred for 3 h at room temperature. A mixture of ether (50 mL) and a 10% HCl solution (59 mL) was added and the resulting organic phase was washed with a 100-mL portion of water. The organic phase was dried over MgSO4, filtered, and concentrated to provide a yellow solid which was recrystallized from ether-hexanes to provide 0.783 g (67%) of a white solid:

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS05861427
Quelldatensatzuspto-grants-1999_01
ORD IDord-5179385bea484e128e58efa202aa4bdd
Quellennotizuspto-grants-1999_01