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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 31229생성일: 2026년 10월 24일

1-Chloro-2,4-Dinitrobenzene → 2,4-Dinitro-1-(2-phenylchroman-6-yloxy)-benzene

https://huagongshe.com/ko/reaction/31229

반응식

참여 물질

역할이름HCID투입량
반응물1-Chloro-2,4-DinitrobenzeneHCID 6—
반응물Potassium HydroxideHCID 14797—
반응물2-Nitro-1-(2-phenylchroman-6-yloxy)-benzeneHCID 17978475—
반응물2-Phenylchroman-6-olHCID 21287538—
용매Dimethyl SulfoxideHCID 679—
생성물2,4-Dinitro-1-(2-phenylchroman-6-yloxy)-benzeneHCID 17978545—

반응 단계

2,4-Dinitro-1-(2-phenylchroman-6-yloxy)-benzene was prepared as described for 2-nitro-1-(2-phenylchroman-6-yloxy)-benzene in Example 29(a) except that 6-hydroxyflavane (0.226 g) was used in 5 ml of dry DMSO under nitrogen. Also KI (0.249 g) and KOH (0.112g) and 2,4-dinitrochlorobenzene (0.210 mg) were added in similar manner. Product was purified by column chromatography (CH2Cl2:n-heptane/75:25 as the eluant). 1H-NMR (400 MHz; d6-DMSO): δ 8.88 (d, 1H, J=2.8 Hz), 8.45 (dd, 1H, J=9.4 Hz, J=2.9 Hz), 7.48-7.30 (m, 5H), 7.14 (d, 1H, J=9.3 Hz), 7.10 (d, 1H, J=2.8 Hz), 7.05 (dd, 1H, J=8.8 Hz, J=2.9 Hz), 6.98 (d, 1H, J=8.7 Hz), 5.16 (dd, 1H, J=10.2 Hz, J=2.1 Hz), 3.08-2.93 (m, 1H), 2.83-2.71 (m, 1H), 2.25-2.13 (m, 1H), 2.08-1.94 (m, 1H).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07425568B2
출처 데이터셋uspto-grants-2008_09
ORD IDord-561a39b5060f4dc4a20e7791a577f847
출처 메모uspto-grants-2008_09