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Sodium sulfate decahydrate → 1-{5-Chloro-2-[(1-methylethyl)sulfanyl]phenyl)methanamine hydrochloride

HRID 1015850
Notizen
Druckvorschau

Reaktionsgleichung

Reaktionsgleichung von HRID 1015850
[H-].[Al+3].[Li+].[H-].[H-].[H-].[Cl:7][C:8]1[CH:9]=[CH:10][C:11]([S:16][CH:17]([CH3:19])[CH3:18])=[C:12]([CH:15]=1)[C:13]#[N:14].O.O.O.O.O.O.O.O.O.O.[O-]S([O-])(=O)=O.[Na+].[Na+]>O1CCCC1>[ClH:7].[Cl:7][C:8]1[CH:9]=[CH:10][C:11]([S:16][CH:17]([CH3:19])[CH3:18])=[C:12]([CH2:13][NH2:14])[CH:15]=1
KomponentenVersuchsvorschriftAufarbeitungQuellen und NachweiseNotizen zur Reaktion

Komponenten

5

Edukt 3

HCID 62649Sodium sulfate decahydrateHCID 21226445Aluminium lithium hydrideHCID 624939095-Chloro-2-[(1-methylethyl)sulfanyl]benzonitrile

Produkt 1

HCID 668785341-{5-Chloro-2-[(1-methylethyl)sulfanyl]phenyl)methanamine hydrochlorideAusbeute 152,1 %

Reagenzien, Katalysatoren, Lösungsmittel 1

HCID 8028
Tetrahydrofuran
Lösungsmittel
2×

Versuchsvorschrift

(Step 2) To a suspension of lithium aluminum hydride (1.56 g) in tetrahydrofuran (250 ml) was added a solution of 5-chloro-2-[(1-methylethyl)sulfanyl]benzonitrile obtained in Step 1 (7.25 g) in tetrahydrofuran (50 ml) at 0° C. The mixture was stirred at room temperature for 3 hr, and treated with sodium sulfate 10 hydrate. The mixture was further stirred at room temperature for 30 min, and the inorganic substance was filtered off through celite. The filtrate was concentrated under reduced pressure. The residue was dissolved in methanol, 4N hydrogen chloride-ethyl acetate solution (15 ml) was added, and the solvent was evaporated under reduced pressure. The obtained solid was washed with a mixed solvent of diisopropyl ether-ethyl acetate to give 1-{5-chloro-2-[(1-methylethyl)sulfanyl]phenyl}methanamine hydrochloride (6.57 g).

Aufarbeitung

  1. stirringThe mixture was further stirred at room temperature for 30 min
  2. filtrationthe inorganic substance was filtered off through celite
  3. concentrationThe filtrate was concentrated under reduced pressure
  4. dissolutionThe residue was dissolved in methanol
  5. addition4N hydrogen chloride-ethyl acetate solution (15 ml) was added
  6. customthe solvent was evaporated under reduced pressure
  7. washThe obtained solid was washed with a mixed solvent of diisopropyl ether-ethyl acetate

Quellen und Nachweise

ORD-Eintrag
ord-da32691a6cb8484aba0ba11b86c84b49
Quelldatensatz
uspto-grants-2011_07
DOI
10.6084/m9.figshare.5104873.v1
Patentnummer
US07985863B2

Notizen zur Reaktion

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