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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 552884생성일: 2026년 10월 26일

Acetonitrile → 3-(2-bromoethyl)Benzofuran

https://huagongshe.com/reaction/552884

반응식

참여 물질

역할이름HCID투입량
반응물AcetonitrileHCID 6342—
반응물2-(Benzofuran-3-yl)ethanolHCID 10953836—
반응물Triphenylphosphane dibromideHCID 12890784—
용매CyclohexaneHCID 8078—
생성물3-(2-bromoethyl)BenzofuranHCID 1507548083.8%

반응 단계

Triphenylphosphane dibromide (5.52 g, 14.4 mmoles) was suspended in abs. acetonitrile (15 ml) under argon, the suspension was brought to 19° C. in a water-bath and 2-(benzofuran-3-yl)ethanol (2.11 g, 13.1 mmoles) in abs. acetonitrile (7 ml) was added in the course of 15 min. During the addition the temperature of the reaction mixture was kept between 19 and 21° C. The mixture was then left to stand for 12 hours without further cooling. The reaction mixture was filtered and the filtrate obtained was concentrated. The residue obtained was taken up in cyclohexane (20 ml), and the mixture was filtered over a silica gel layer (15 g) about 3 cm thick. The silica gel was washed with cyclohexane (5×20 ml) and the filtrate obtained was concentrated. 2.47 g 3-(2-bromoethyl)benzofuran were obtained as a yellowish oil.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07951948B2
출처 데이터셋uspto-grants-2011_05
ORD IDord-f518eaf3333d4209b8d56185110bbe4a
출처 메모uspto-grants-2011_05