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HRID 1106389Erstellt: 25. Oktober 2026

1,3,5-Tribromobenzene → 1,3-Dibromo-5-dimesitylborylbenzene

https://huagongshe.com/reaction/1106389

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
Edukt1,3,5-TribromobenzeneHCID 12279—
EduktDimesitylboron fluorideHCID 3466040—
EduktButyllithiumHCID 178418339—
LösungsmittelDiethyl EtherHCID 3283—
LösungsmittelHexaneHCID 8058—
Produkt1,3-Dibromo-5-dimesitylborylbenzeneHCID 18787953—

Reaktionsbedingungen

Temperatur-78 °C

Reaktionsschritte

6.25 ml (0.01 mol) of 1.6 M butyllithium in hexane are added over 5 minutes at -78° C. to a suspension of 3.14 g (0.01 mol) of 1,3,5-tribromobenzene in 50 ml of diethyl ether. The reaction mixture is stirred at -78° C. for 2 hours, during which a yellow-orange suspension is produced. 2.68 g (0.01 mol) of solid dimesitylfluoroborane are added, and the reaction mixture is warmed to room temperature over about one hour. The mixture is then diluted with 50 ml of hexane and cooled to 0° C. The solid produced is filtered, washed several times with cold hexane and then washed with water and, finally, with methanol, until the solid is colourless. Drying gives 3.54 g (0.0073 mol; i.e. 73% of theory) of a white solid (1,3-dibromo-5-dimesitylborylbenzene). Following purification by chromatography (hexane; SiO2) a melting point of 190-191° C. is obtained. Elemental analysis for C24H25BBr2 gives: C calc.: 59.55%; found: 59.52% H calc.: 5.21%; found: 5,12%

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS06057078
Quelldatensatzuspto-grants-2000_05
ORD IDord-6cdf08e273dc4f4ab05442fc9db2968a
Quellennotizuspto-grants-2000_05