Nitroethane → 1,2,4,5-Tetrafluoro-3-(2-nitroprop-1-enyl)benzene

HRID 920456

Reaktionsgleichung

[F:1][C:2]1[C:9]([F:10])=[CH:8][C:7]([F:11])=[C:6]([F:12])[C:3]=1[CH:4]=O.[N+:13]([CH2:16][CH3:17])([O-:15])=[O:14].C1(N)CCCCC1>C(O)(=O)C>[F:11][C:7]1[CH:8]=[C:9]([F:10])[C:2]([F:1])=[C:3]([CH:4]=[C:16]([N+:13]([O-:15])=[O:14])[CH3:17])[C:6]=1[F:12]

Komponenten

Reaktionsbedingungen

Temperatur: 80 °C

Versuchsvorschrift

A mixture of 2,3,5,6-tetrafluorobenzaldehyde (25.0 g, 0.14 mol), nitroethane (21.08 g, 0.28 mol), and cyclohexylamine (13.92 g, 0.14 mol) in 150 mL of acetic acid was heated at 80° C. for 5-6 h under an argon atmosphere. After the end of the reaction was established by TLC, the reaction mixture was cooled to room temperature (rt) and the solvent was removed under vacuum. The residue was diluted with water, extracted with ethyl acetate three times. The combined extracts were dried over anhydrous MgSO4, filtered, and concentrated under vacuum. Product was purified by a silica gel chromatography using ethyl acetate and hexanes (1:6 to 1:4) as eluent to afford 30.0 g (91%) of the designed compound as yellow solid. Mass (ESI, positive) m/z 258.0 [M+Na]+.

Aufarbeitung

temperaturethe reaction mixture was cooled to room temperature (rt)
customthe solvent was removed under vacuum
additionThe residue was diluted with water
extractionextracted with ethyl acetate three times
dry with materialThe combined extracts were dried over anhydrous MgSO4
filtrationfiltered
concentrationconcentrated under vacuum
customProduct was purified by a silica gel chromatography

Quellen und Nachweise

ORD-Eintrag: ord-c14df3aa857842d59c81a52809e59ef6
Quelldatensatz: uspto-grants-2016_03
DOI: 10.6084/m9.figshare.5104873.v1
Patentnummer: US09273055B2

Verknüpfte Notizen

Wird geladen…