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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 412696생성일: 2026년 10월 24일

Sodium hydride → 4-(4-Phenylbutoxy)-1,2-dinitrobenzene

https://huagongshe.com/ko/reaction/412696

반응식

참여 물질

역할이름HCID투입량
반응물Sodium hydrideHCID 24758—
반응물4-Chloro-1,2-dinitrobenzeneHCID 33097—
반응물BenzenebutanolHCID 76889—
용매TetrahydrofuranHCID 8028—
생성물4-(4-Phenylbutoxy)-1,2-dinitrobenzeneHCID 1853791372%

반응 단계

4-Phenyl-1-butanol (1 mL, 6.49 mmol) in THF (3 mL) was combined under dry nitrogen with sodium hydride (0.26 g, 6.5 mmol) in a 60% mineral oil dispersion. The mixture was stirred vigorously for 5 minutes, combined with 3,4-dinitrochlorobenzene (1.3 g, 6.42 mmol) and then stirred 10 hours at room temperature. The mixture was partitioned between diethyl ether and 3N hydrochloric acid. The aqeuous layer was separated and extracted several times with diethyl ether. The combined organic layers were dried (MgSO4), filtered and concentrated by rotary evaporation. The residue was purfied by flash chromatography (9:1 hexanes/diethyl ether) to provide 4-(4-phenylbutoxy)-1,2-dinitrobenzene (1.16 g, 72% yield); 1H-NMR (300 Mhz, CDCL3): 7.84 (d, 1H, J=10.0 Hz), 7.19-7.36 (m, 5H), 7.00-7.06 (m, 2H), 4.10 (t, 2H, J=5.7 Hz), 2.73 (t, 2H, J=6.5 Hz), 1.89 (m, 4H).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06562854B2
출처 데이터셋uspto-grants-2003_05
ORD IDord-18edf7757a4747c7a02c3776e4fa8613
출처 메모uspto-grants-2003_05