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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1082007Erstellt: 24. Oktober 2026

4-Bromotoluene → 4,4-Dimethyl-2-(4'-methyl-2-biphenylyl)-2-oxazoline

https://huagongshe.com/de/reaction/1082007

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
Edukt4-BromotolueneHCID 7805—
Edukt1,1-DibromoethaneHCID 11201—
EduktAmmonium ChlorideHCID 25517—
Edukt4,4-Dimethyl-2-(2-methoxyphenyl)oxazolineHCID 333189—
EduktMagnesiumHCID 5462224—
LösungsmittelTetrahydrofuranHCID 8028—
Produkt4,4-Dimethyl-2-(4'-methyl-2-biphenylyl)-2-oxazolineHCID 68830185,1%

Reaktionsschritte

Tetrahydrofuran (200 ml) was added to 2.5 g (103 mmol) of flaky magnesium, followed by the addition of a small amount of dibromoethane under stirring. After the confirmation of bubbling, 13 ml (106 mmol) of 4-bromotoluene was dropwise added thereto. After the confirmation of the dissolution of the magnesium, the mixture was further stirred at room temperature for one hour. This reaction liquid was dropwise added to a solution of 10.0 g (48.7 mmol) of 4,4-dimethyl-2-(2'-methoxyphenyl)oxazoline in tetrahydrofuran (100 ml), followed by stirring for 12 hours. The reaction liquid was poured into a saturated aqueous solution of ammonium chloride, followed by the extraction with chloroform. After washing with water and drying, vacuum concentration was conducted. The residue was purified by silica gel column chromatography (a n-hexane/ethyl acetate system) to give 11.0 g of the title compound as a crystal (yield 85%).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS05587504
Quelldatensatzuspto-grants-1996_12
ORD IDord-b6d7fe66299b4e768f150946ef2e1a36
Quellennotizuspto-grants-1996_12