Sodium Dithionite → HCID 86665284, Verbindung

HRID 1970844Notizen

Reaktionsgleichung

Reaktionsgleichung von HRID 1970844
[CH3:1][O:2][C:3]1[CH:8]=[CH:7][CH:6]=[C:5]([CH3:9])[C:4]=1[NH2:10].I[C:12]([F:24])([C:17]([F:23])([F:22])[C:18]([F:21])([F:20])[F:19])[C:13]([F:16])([F:15])[F:14].S(S([O-])=O)([O-])=O.[Na+].[Na+].C(=O)([O-])O.[Na+]>O.COC(C)(C)C.S([O-])(O)(=O)=O.C([N+](CCCC)(CCCC)CCCC)CCC>[F:24][C:12]([C:7]1[CH:6]=[C:5]([CH3:9])[C:4]([NH2:10])=[C:3]([O:2][CH3:1])[CH:8]=1)([C:13]([F:14])([F:15])[F:16])[C:17]([F:22])([F:23])[C:18]([F:21])([F:20])[F:19]

Komponenten

8

Versuchsvorschrift

To a solution of 2-methoxy-6-methylphenylamine (8.23 g, 60 mmol) in a mixture of water (60 ml) and tert-butyl methyl ether (60 ml) was added, successively 2-iodononafluorobutane (24.9 g, 11.86 ml, 72 mmol), sodium hydrosulfite (15.29 g, 72 mmol), sodium hydrogen carbonate (6.05 g, 72.0 mmol) and tetrabutyl ammonium hydrogen sulfate (“TBAHS”) (2.24 g, 6.60 mmol). The reaction mixture was stirred at ambient temperature for 16 hours. The mixture was filtered and the filtrate was extracted twice with tert-butyl methyl ether. The combined organic phases were washed with aqueous hydrochloric acid (1N), dried over sodium sulfate and concentrated to give 4-(1,2,2,3,3,3-hexafluoro-1-trifluoromethylpropyl)-2-methoxy-6-methylphenylamine which was used without further purification. LC-MS (Method 2): RT=2.05, [M+H]+=356.

Aufarbeitung

  1. additionwas added
  2. filtrationThe mixture was filtered
  3. extractionthe filtrate was extracted twice with tert-butyl methyl ether
  4. washThe combined organic phases were washed with aqueous hydrochloric acid (1N)
  5. dry with materialdried over sodium sulfate
  6. concentrationconcentrated

Quellen und Nachweise

ORD-Eintrag
ord-0fd4a1254fa846899ab4aca769a3f260
Quelldatensatz
uspto-grants-2013_04
Patentnummer
US08431514B2

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