돌아가기
Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 341600생성일: 2026년 10월 26일

3-(3-Bromophenyl)acrylic acid → 3-(3-Bromophenyl)propan-1-ol

https://huagongshe.com/reaction/341600

반응식

참여 물질

역할이름HCID투입량
반응물3-(3-Bromophenyl)acrylic acidHCID 36251—
반응물Aluminium lithium hydrideHCID 21226445—
용매Diethyl EtherHCID 3283—
생성물3-(3-Bromophenyl)propan-1-olHCID 18785928—

반응 단계

To suspension of LiAlH4 (0.5 g, 1.3 mmol) in diethyl ether (25 mL) was added 3-bromocinnamic acid (83, 1.0 g, 4 mmol), in portions, at RT. The resulting suspension was stirred for 3 hours. The reaction was quenched by the successive addition of 15% aq. NaOH solution (1 mL) and water. The resulting white suspension was filtered through a pad of Celite. The filter cake was washed with ether and then ethyl acetate. The filtrate was concentrated to afford crude 8 as yellow oil. Yield (0.7 g, 74%). 1H NMR (400 MHz, CDCl3) δ 7.10-7.35 (m, 4H), 3.65 (t, J=6.5 Hz, 2H), 2.68 (t, J=7.8 Hz, 2H), 1.82-1.91 (m, 2H).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08895782B2
출처 데이터셋uspto-grants-2014_11
ORD IDord-113ab9c4c4c24bfc93cd3d93b4ee7f3a
출처 메모uspto-grants-2014_11