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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 2091713Erstellt: 26. Oktober 2026

Carbon tetrabromide → 1-Bromo-4-(bromomethyl)-2,5-difluorobenzene

https://huagongshe.com/reaction/2091713

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktCarbon tetrabromideHCID 11205—
EduktTriphenylphosphineHCID 11776—
Edukt(4-Bromo-2,5-difluorophenyl)methanolHCID 53401418—
LösungsmittelDichloromethaneHCID 6344—
Produkt1-Bromo-4-(bromomethyl)-2,5-difluorobenzeneHCID 2191121087,4%

Reaktionsschritte

To a solution of 2 g (8.44 mmol) of 4-bromo-2,5-difluorobenzoic acid (prepared according to the procedure of Ishikawa et al., Kogyo Kagaku Zasshi, pg 972-979, 1970) in 20 mL of tetrahydrofuran was added 40 mL of a 1M solution of borane-tetrahydrofuran complex. The solution was heated under reflux for 64 h, cooled to ambient temperature and 100 mL of methanol was added. The reaction was then heated for a further 2 h, cooled and concentrated in vacuo. Purification by flash chromatography (silica gel, 9:1 hexane:ethyl acetate) afforded 1.6 g of 4-bromo-2,5-difluorobenzyl alcohol. To a solution of 1.3 g (5 6 mmol) of 4-bromo-2,5-difluorobenzyl alcohol in 20 mL of dichloromethane at 0° C. was added 2.27 g (6.7 mmol) of carbon tetrabromide and 1.8 g (6.7 mmol) of triphenylphosphine. The reaction was stirred for 2 h at this temperature, the solvent was removed in vacuo and the residue stirred with 100 mL of diethyl ether. The solution was filtered, concentrated in vacuo, and purified by flash chromatography (silica gel, 9:1 hexane:ethyl acetate) to afford 1.5 g of the title compound.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08440668B2
Quelldatensatzuspto-grants-2013_05
ORD IDord-abf58ba0abe6453b92b1adbf44f3a927
Quellennotizuspto-grants-2013_05