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Potassium Carbonate → HCID 59427967, Verbindung

HRID 2115872
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Druckvorschau

Reaktionsgleichung

Reaktionsgleichung von HRID 2115872
[Cl:1][C:2]1[CH:7]=[C:6]([C:8]([F:11])([F:10])[F:9])[CH:5]=[C:4]([N+:12]([O-])=O)[C:3]=1F.C([O-])([O-])=O.[K+].[K+].[CH3:22][N:23]([CH3:29])[CH2:24][CH2:25][CH2:26][NH:27][CH3:28]>C1COCC1>[Cl:1][C:2]1[CH:7]=[C:6]([C:8]([F:11])([F:10])[F:9])[CH:5]=[C:4]([NH2:12])[C:3]=1[N:27]([CH2:26][CH2:25][CH2:24][N:23]([CH3:29])[CH3:22])[CH3:28]
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Komponenten

5

Edukt 3

HCID 11430Potassium CarbonateHCID 783021,3-Propanediamine, N1,N1,N3-trimethyl-HCID 27365653-Chloro-4-fluoro-5-nitrobenzotrifluoride

Produkt 1

HCID 59427967HCID 59427967, Verbindung

Reagenzien, Katalysatoren, Lösungsmittel 1

HCID 8028TetrahydrofuranLösungsmittel

Versuchsvorschrift

A heterogeneous mixture of 1-chloro-2-fluoro-3-nitro-5-(trifluoromethyl)benzene (1.25 mL, 8.2 mmol), K2CO3 (3.44 g, 24.6 mmol), N1,N1,N3-trimethylpropane-1,3-diamine (1.26 mL, 8.61 mmol) and THF were allowed to stir at RT for 45 min. The THF was removed under reduced pressure and reconstituted in EtOAc (50 ml). The organic layer was washed with water (20 ml), brine (20 ml), dried over anhydrous sodium sulfate, filtered and concentrated to an oil. The concentrated oil was taken up in EtOH (20 ml) to which Raney nickel (2.5 g wet, washed) was added. The reduction was monitored and after 1 h, another portion of Raney nickel (3.8 g, wet, washed) was added. The reaction was allowed to stir for an additional 30 min., and filtered through Celite, washed with EtOH (10 mL) and concentrated. The crude residue was purified via flash chromatography (silica gel, gradient elution 0 to 25% MeOH in CH2Cl2) to afford 6-chloro-N1-(3-(dimethylamino)propyl)-N1-methyl-4-(trifluoromethyl)benzene-1,2-diamine as a yellow oil. MS m/z=310.1 [M+H]+. Calc'd for C13H19ClF3N3: 309.8.

Aufarbeitung

  1. customThe THF was removed under reduced pressure
  2. washThe organic layer was washed with water (20 ml), brine (20 ml)
  3. dry with materialdried over anhydrous sodium sulfate
  4. filtrationfiltered
  5. concentrationconcentrated to an oil
  6. additionwas added
  7. waitThe reduction was monitored and after 1 h
  8. additionanother portion of Raney nickel (3.8 g, wet, washed) was added
  9. stirringto stir for an additional 30 min.
  10. filtrationfiltered through Celite
  11. washwashed with EtOH (10 mL)
  12. concentrationconcentrated
  13. customThe crude residue was purified via flash chromatography (silica gel, gradient elution 0 to 25% MeOH in CH2Cl2)

Quellen und Nachweise

ORD-Eintrag
ord-0c647f16f7e74af89039fede96eda6f1
Quelldatensatz
uspto-grants-2008_10
DOI
10.6084/m9.figshare.5104873.v1
Patentnummer
US07435823B2

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