Hexane → 1-[1-(4-cyanophenyl)4-(4-fluorophenyl)butyl]-1H-imidazole

HRID 1737858

Reaktionsgleichung

[C:1]([C:3]1[CH:14]=[CH:13][C:6]([CH2:7][N:8]2[CH:12]=[CH:11][N:10]=[CH:9]2)=[CH:5][CH:4]=1)#[N:2].[Li]CCCC.CCCCCC.[F:26][C:27]1[CH:32]=[CH:31][C:30]([CH2:33][CH2:34][CH2:35]Br)=[CH:29][CH:28]=1.[Cl-].[NH4+]>C1COCC1>[C:1]([C:3]1[CH:4]=[CH:5][C:6]([CH:7]([N:8]2[CH:12]=[CH:11][N:10]=[CH:9]2)[CH2:35][CH2:34][CH2:33][C:30]2[CH:31]=[CH:32][C:27]([F:26])=[CH:28][CH:29]=2)=[CH:13][CH:14]=1)#[N:2]

Komponenten

Reaktionsbedingungen

Temperatur: -70 °C

Versuchsvorschrift

1-(4-cyanobenzyl)-imidazole (1 g, 0.0054 mol) is dissolved into dry tetrahydrofuran (30 ml) and cooled to -70° C. n-BuLi in hexane (0.0054 mol) is added dropwise into the reaction mixture. After stirring for additional 30 min at -70° C. 3-(4-fluorophenyl)propyl bromide (1.5 g, 0.0069 mol) in THF (10 ml) is added to the mixture and stirig is continued for 2 hours. Then the mixture is allowed to warm to room temperature. Saturted aqueous ammonium chloride solution is added to the mixture, shaked and then the layers are separated. THF-phase is dried and evaporated to dryness. The residue is crystalizd from isopropanol as hydrogen chloride salt. The filtrate is purified by flash chromatography.

Aufarbeitung

additionis added dropwise into the reaction mixture
waitis continued for 2 hours
temperatureto warm to room temperature
customshaked and then the layers are separated
dry with materialTHF-phase is dried
customevaporated to dryness
customThe filtrate is purified by flash chromatography

Quellen und Nachweise

ORD-Eintrag: ord-a37b8f5ca0db421ba5455d1607c863bc
Quelldatensatz: uspto-grants-1999_10
DOI: 10.6084/m9.figshare.5104873.v1
Patentnummer: US05962495

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