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Ammonium Chloride → HCID 82374291, Verbindung

HRID 2091307
Notizen
Druckvorschau

Reaktionsgleichung

Reaktionsgleichung von HRID 2091307
[CH3:1][C:2]1[C:10]2[C:5](=[N:6][CH:7]=[CH:8][CH:9]=2)[S:4][C:3]=1[C:11](OCC)=[O:12].[Cl-].[Ca+2].[Cl-].[BH4-].[Na+].[Cl-].[NH4+]>O1CCCC1.[O-2].[O-2].[Mn+4].C(O)C>[CH3:1][C:2]1[C:10]2[C:5](=[N:6][CH:7]=[CH:8][CH:9]=2)[S:4][C:3]=1[CH:11]=[O:12]
KomponentenVersuchsvorschriftAufarbeitungQuellen und NachweiseNotizen zur Reaktion

Komponenten

8

Edukt 4

HCID 25517Ammonium ChlorideHCID 4311764Sodium borohydrideHCID 5284359Calcium ChlorideHCID 46941714HCID 46941714, Verbindung

Produkt 1

HCID 82374291HCID 82374291, VerbindungAusbeute 86,2 %

Reagenzien, Katalysatoren, Lösungsmittel 3

HCID 178418406
HCID 178418406, Verbindung
Katalysator
HCID 702EthanolLösungsmittel
HCID 8028TetrahydrofuranLösungsmittel2×

Versuchsvorschrift

To a mixture of ethyl 3-methylthieno[2,3-b]pyridine-2-carboxylate (3.00 g) synthesized above, calcium chloride (3.02 g), ethanol (50 mL) and tetrahydrofuran (50 mL) was added sodium borohydride (2.06 g) at 0° C., and the mixture was stirred at room temperature for 4 hr. Saturated aqueous ammonium chloride solution was added to quench the reaction, and the reaction mixture was extracted with ethyl acetate. The extract was washed with saturated brine, dried over magnesium sulfate, and concentrated under reduced pressure to give a white solid. To a solution (50 mL) of the obtained solid in tetrahydrofuran was added active manganese dioxide (12.5 g), and the mixture was stirred at 50° C. overnight. Manganese dioxide was filtered off, and the filtrate was concentrated under reduced pressure. The residue was washed with diisopropyl ether to give the title object compound (2.07 g, 86%) as a pale-yellow solid.

Aufarbeitung

  1. customto quench
  2. customthe reaction
  3. extractionthe reaction mixture was extracted with ethyl acetate
  4. washThe extract was washed with saturated brine
  5. dry with materialdried over magnesium sulfate
  6. concentrationconcentrated under reduced pressure
  7. customto give a white solid
  8. stirringthe mixture was stirred at 50° C. overnight
  9. filtrationManganese dioxide was filtered off
  10. concentrationthe filtrate was concentrated under reduced pressure
  11. washThe residue was washed with diisopropyl ether

Quellen und Nachweise

ORD-Eintrag
ord-2bee959aa0b84303b4d0a3af39f4f681
Quelldatensatz
uspto-grants-2013_05
DOI
10.6084/m9.figshare.5104873.v1
Patentnummer
US08436043B2

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