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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 31225생성일: 2026년 10월 23일

Dichloromethane → 2-Nitro-1-(2-phenylchroman-6-yloxy)-benzene

https://huagongshe.com/ko/reaction/31225

반응식

참여 물질

역할이름HCID투입량
반응물DichloromethaneHCID 6344—
반응물1-Chloro-2-nitrobenzeneHCID 6945—
반응물Potassium HydroxideHCID 14797—
반응물2-Phenylchroman-6-olHCID 21287538—
용매Dimethyl SulfoxideHCID 679—
생성물2-Nitro-1-(2-phenylchroman-6-yloxy)-benzeneHCID 17978475—

반응 단계

6-Hydroxyflavane (0.150 g) was dissolved in dry DMSO (5 ml) under nitrogen. KI (0.166 g) and KOH (0.074g) were added and solution was stirred at room temperature for 15 minutes. 2-Chloro-1-nitrobenzene (0.104 g) was added and the solution was stirred at +90° C. for 2.5 hours. Cooled solution was taken up with CH2Cl2 and washed with H2O and 2M NaOH. Phases were separated and water phase was washed CH2Cl2. All organic phases were combined and washed with 1M HCl and then H2O (until pH˜7) and brine. Solution was dried over Na2SO4 and purified with filtration through the small silica column in CH2Cl2:n-heptane (60:40). 1H-NMR (300 MHz; d6-DMSO): δ 8.01 (dd, 1H, J=8.1 Hz; J=1.7 Hz), 7.69 (m, 1H), 7.50-7.31 (m, 5H), 7.31-7.24 (m, 1H), 7.04 (dd, 1H, J=8.5 Hz; J=1.2 Hz), 6.92 (s, 1H), 6.90 (s, 2H), 5.12 (dd, 1H, J=10.1 Hz; J=2.3 Hz), 2.95 (ddd, 1H, J=16.9 Hz; J=11.2 Hz, J=5.8 Hz), 2.73 (ddd, 1H, J=16.9 Hz; J=3.2 Hz, J=1.7 Hz), 2.25-2.10 (m, 1H), 2.08-1.90 (m, 1H).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07425568B2
출처 데이터셋uspto-grants-2008_09
ORD IDord-d43da5d2175a43c7bb5ecbd4fc202682
출처 메모uspto-grants-2008_09