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HRID 1445768作成日:2026年10月27日

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

https://huagongshe.com/reaction/1445768

反応式

関与物質

役割名称HCID仕込み量
反応物AcetonitrileHCID 6342—
反応物2,8,9-Trimethyl-2,5,8,9-tetraaza-1-phosphabicyclo(3.3.3)undecaneHCID 4186723—
反応物2-(4-Bromo-phenyl)-4-(2-iodo-ethyl)-5-methyl-oxazoleHCID 58951394—
溶媒TetrahydrofuranHCID 8028—
生成物2-(4-Bromo-phenyl)-5-methyl-4-vinyl-oxazoleHCID 2226115583%

反応手順

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).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07666871B2
出典データセットuspto-grants-2010_02
ORD IDord-ba4c2a92eedd4af18842cbe06c550aa2
出典メモuspto-grants-2010_02