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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1740284Erstellt: 26. Oktober 2026

Hydrochloric Acid → 3,5-Dichlorophenylboronic acid

https://huagongshe.com/reaction/1740284

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktHydrochloric AcidHCID 313—
EduktTriisopropyl borateHCID 21531—
EduktBenzene, 1-bromo-3,5-dichloro-HCID 29766—
EduktButyllithiumHCID 178418339—
LösungsmittelTetrahydrofuranHCID 8028—
LösungsmittelHexaneHCID 8058—
Produkt3,5-Dichlorophenylboronic acidHCID 2734331—

Reaktionsbedingungen

Temperatur-78 °C

Reaktionsschritte

To a cold (-78° C.) solution of 1-bromo-3,5-dichlorobenzene (14 g) and triisopropoxyborane (20.8 ml) in tetrahydrofuran (140 ml) was added dropwise n-butyllithium in hexane (1.66 M, 52.3 ml). The mixture was stirred at -78° C. for one hour and warmed to room temperature over two hours. The reaction mixture was poured onto 2M hydrochloric acid solution (120 ml) and stirred for 10 minutes. The product was extracted with ether (200 ml) 3 times, and the organic layers were combined, washed with brine, dried over magnesium sulfate and evaporated in vacuo. To the residue was added petroleum ether and the crystalline was collected, washed with petroleum ether and dried to give 3,5-dichlorophenyl-dihydroxyborane.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS05968985
Quelldatensatzuspto-grants-1999_10
ORD IDord-3b868a2f93d7475d853d55e381fe8c10
Quellennotizuspto-grants-1999_10