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HRID 1445768생성일: 2026년 10월 26일

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

https://huagongshe.com/reaction/1445768

반응식

참여 물질

역할이름HCID투입량
반응물AcetonitrileHCID 6342—
반응물2,8,9-Trimethyl-2,5,8,9-tetraaza-1-phosphabicyclo(3.3.3)undecaneHCID 4186723—
반응물2-(4-Bromo-phenyl)-4-(2-iodo-ethyl)-5-methyl-oxazoleHCID 58951394—
용매TetrahydrofuranHCID 8028—
생성물2-(4-Bromo-phenyl)-5-methyl-4-vinyl-oxazoleHCID 2226115583%

반응 단계

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).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07666871B2
출처 데이터셋uspto-grants-2010_02
ORD IDord-ba4c2a92eedd4af18842cbe06c550aa2
출처 메모uspto-grants-2010_02