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Potassium Carbonate → HCID 59427967、化合物

HRID 1042667
ノート
印刷プレビュー

反応式

HRID 1042667 の反応式
[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]
参加物実験手順後処理出典と根拠反応ノート

参加物

5

反応物 3

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

生成物 1

HCID 59427967HCID 59427967、化合物

試薬・触媒・溶媒 1

HCID 8028Tetrahydrofuran溶媒

実験手順

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 room temperature 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.

後処理

  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)

出典と根拠

ORDレコード
ord-310a745a8a11430f948020336023e5b3
出典データセット
uspto-grants-2013_10
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US08557996B2

反応ノート

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