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HRID 1445768Erstellt: 26. Oktober 2026

Acetonitrile → 2-(4-Bromo-phenyl)-5-methyl-4-vinyl-oxazole

https://huagongshe.com/reaction/1445768

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktAcetonitrileHCID 6342—
Edukt2,8,9-Trimethyl-2,5,8,9-tetraaza-1-phosphabicyclo(3.3.3)undecaneHCID 4186723—
Edukt2-(4-Bromo-phenyl)-4-(2-iodo-ethyl)-5-methyl-oxazoleHCID 58951394—
LösungsmittelTetrahydrofuranHCID 8028—
Produkt2-(4-Bromo-phenyl)-5-methyl-4-vinyl-oxazoleHCID 2226115583%

Reaktionsschritte

Add 2,8,9-trimethyl-2,5,8,9-tetraaza-1-phosphabicyclo[3.3.3]undecane (3.17 g, 14.7 mmol) as a solution using acetonitrile (10 mL) to a solution of 2-(4-bromo-phenyl)-4-(2-iodo-ethyl)-5-methyl-oxazole (See Intermediate 30) (4.38 g, 11.1 mmol) in 2.8:1 acetonitrile:THF (190 mL). After 4 hrs, concentrate under reduced pressure and add EtOAc and water to the residue. Separate the layers and extract the aqueous material with EtOAc. Wash the crude organic extract with water, dry over MgSO4, filter and concentrate. Purify on silica gel eluting with 7% EtOAc to give 2-(4-bromo-phenyl)-5-methyl-4-vinyl-oxazole (2.31 g, 83%): 1H NMR (400 Hz): (CDCl3) δ 7.89 (d, 2H, J=8 Hz), 7.57 (d, 2H, J=8 Hz), 6.54 (dd, 1H, J=17, 11 Hz), 5.93 (dd, 1H, J=17, 2 Hz), 5.29 (dd, 1H, J=11, 2 Hz), 2.40 (s, 3H).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07666871B2
Quelldatensatzuspto-grants-2010_02
ORD IDord-ba4c2a92eedd4af18842cbe06c550aa2
Quellennotizuspto-grants-2010_02