돌아가기
Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1373766생성일: 2026년 10월 26일

Allyl bromide → 2-(Allyloxy)-1-bromo-5-methyl-3-nitrobenzene

https://huagongshe.com/reaction/1373766

반응식

참여 물질

역할이름HCID투입량
반응물Allyl bromideHCID 7841—
반응물Potassium CarbonateHCID 11430—
반응물2-Bromo-4-methyl-6-nitrophenolHCID 29918—
용매AcetoneHCID 180—
생성물2-(Allyloxy)-1-bromo-5-methyl-3-nitrobenzeneHCID 1497744494.2%

반응 단계

To a mixture of 2-bromo-4-methyl-6-nitrophenol (7.00 g, 30.2 mmol), K2CO3 (6.26 g, 45.3 mmol) in acetone (105 mL) was added allyl bromide (3.80 ml, 45.3 mmol). The reaction mixture was stirred at room temperature overnight. It was then heated at 40° C. for 5 hrs. Inorganic salts were filtered and washed with acetone. The filtrate was concentrated to give 7.74 g (94%) of the desired product. MS (DCI/NH3) m/z: 289.0 (M+NH4)+; 1H NMR (300 MHz, CD3OD) δ ppm 2.37 (s, 3 H) 4.61 (d, J=6.10 Hz, 2 H) 5.26 (dd, J=10.51, 1.80 Hz, 1 H) 5.39 (dd, J=17.29, 1.80 Hz, 1 H) 6.09 (m, 1 H) 7.63 (s, 1 H) 7.74 (s, 1 H).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07163939B2
출처 데이터셋uspto-grants-2007_01
ORD IDord-45249ef8d80d45258c2767c58c8dce87
출처 메모uspto-grants-2007_01