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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 546396생성일: 2026년 10월 26일

Methanol → 2-Styryloxazole-4-carbaldehyde

https://huagongshe.com/reaction/546396

반응식

참여 물질

역할이름HCID투입량
반응물MethanolHCID 887—
반응물ethyl 2-[(E)-2-phenylethenyl]-1,3-oxazole-4-carboxylateHCID 5708074—
반응물DiisobutylaluminumhydrideHCID 21225700—
용매DichloromethaneHCID 6344—
생성물2-Styryloxazole-4-carbaldehydeHCID 1173577783.5%

반응 단계

Diisobutylaluminum hydride (1.0N hexane solution, 66 ml) was added dropwise to a solution of 4-ethoxycarbonyl-2-(trans-styryl)oxazole (8.57 g) in dichloromethane (80 ml) at −78° C. After 15 minutes, methanol (11 ml) was added dropwise, and the mixture was warmed to room temperature over 1 hour. The reaction mixture was filtered through Celite, and the resultant pasty substance was dissolved in ethyl acetate (200 ml) and a saturated aqueous solution (200 ml) of ammonium chloride was added, and an organic layer was separated. The water layer was then extracted with dichloromethane (2×100 ml). The resultant organic layers were collected and washed with a saturated aqueous solution (100 ml) of sodium hydrogencarbonate and saturated saline (100 ml), combined with the filtrate obtained by the filtration through Celite and then dried over anhydrous sodium sulfate, and the solvent was distilled off under reduced pressure. The residue was purified by column chromatography on silica gel (dichloromethane:ethyl acetate=5:1→dichloromethane:methanol=10:1) to obtain the title compound (5.86 g) as colorless needle crystals.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07935824B2
출처 데이터셋uspto-grants-2011_05
ORD IDord-faa51eafda2a426e8a303e5a5091b2a3
출처 메모uspto-grants-2011_05