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HRID 412696作成日:2026年10月25日

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

https://huagongshe.com/reaction/412696

反応式

関与物質

役割名称HCID仕込み量
反応物Sodium hydrideHCID 24758—
反応物4-Chloro-1,2-dinitrobenzeneHCID 33097—
反応物BenzenebutanolHCID 76889—
溶媒TetrahydrofuranHCID 8028—
生成物4-(4-Phenylbutoxy)-1,2-dinitrobenzeneHCID 1853791372%

反応手順

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).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US06562854B2
出典データセットuspto-grants-2003_05
ORD IDord-18edf7757a4747c7a02c3776e4fa8613
出典メモuspto-grants-2003_05