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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 466643Erstellt: 23. Oktober 2026

3-Bromobenzaldehyde → 1-Bromo-3-(2-methyl-1-propenyl)benzene

https://huagongshe.com/de/reaction/466643

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
Edukt3-BromobenzaldehydeHCID 76583—
EduktIsopropyltriphenylphosphonium iodideHCID 2723783—
EduktPotassium tert-butoxideHCID 23665647—
Katalysator18-Crown-6HCID 28557—
LösungsmittelTetrahydrofuranHCID 8028—
Produkt1-Bromo-3-(2-methyl-1-propenyl)benzeneHCID 2170683675,3%

Reaktionsschritte

To a stirred slurry of 17.83 g (41.2 mmol) of isopropyltriphenylphosphonium iodide and 300 mg (1.1 mmol) of 18-crown-6 in 50 mL of THF under nitrogen at 5° C. was added 4.60 g (41.0 mmol) of potassium t-butoxide over 5 minutes. The resulting deep red-orange slurry was stirred 10 minutes and then a solution of 4.31 mL (37.0 mmol) of 3-bromobenzaldehyde in 40 mL of THF was added at a rate to keep the temperature below 10° C. The resulting bright yellow slurry was stirred for 20 minutes and then poured into 300 mL of hexanes. The solids were filtered off and the filtrate evaporated. This residue was purified by flash chromatography (5×15 cm column) and eluted with hexanes to provide 5.88 g (75%) of title compound as a colorless oil.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS05157027
Quelldatensatzuspto-grants-1992_10
ORD IDord-2e4bd4a7bf1b4401a81feba32fb102f2
Quellennotizuspto-grants-1992_10