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HRID 43052作成日:2026年10月25日

1-Fluoro-3-nitrobenzene → 1-Ethyl-4-(3-nitrophenyl)piperazine

https://huagongshe.com/reaction/43052

反応式

関与物質

役割名称HCID仕込み量
反応物1-Fluoro-3-nitrobenzeneHCID 9823—
反応物1-EthylpiperazineHCID 79196—
溶媒WaterHCID 962—
溶媒Dichloromethane methanolHCID 21226129—
生成物1-Ethyl-4-(3-nitrophenyl)piperazineHCID 5823598585.9%

反応手順

A mixture of 2-fluoro-4-nitrobenzene (3.2 mL, 29.7 mmol) and 1-ethylpiperazine (7.6 mL, 59.4 mmol, 2 equiv) was heated to reflux for 117 h. After cooling to rt, the reaction mixture was diluted with H2O and DCM/MeOH, 9:1. The aqueous layer was separated and extracted with DCM/MeOH, 9:1. The organic phase was washed with brine, dried (Na2SO4), filtered and concentrated. Purification of the residue by silica gel column chromatography (DCM/MeOH, 1:0→95:5) afforded 6 g of the title compound as a brown oil: ESI-MS: 236.0 [M+H]+; tR=2.49 min (System 1); TLC: Rf=0.26 (DCM/MeOH, 95:5).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08536175B2
出典データセットuspto-grants-2013_09
ORD IDord-9fb70e2a006546babb2dbf95ec279807
出典メモuspto-grants-2013_09