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Ammonium Chloride → 3-Methylthieno[2,3-c]pyridine-2-carbaldehyde

HRID 2091287
Notizen
Druckvorschau

Reaktionsgleichung

Reaktionsgleichung von HRID 2091287
[CH3:1][C:2]1[C:10]2[C:5](=[CH:6][N: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](=[CH:6][N: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 46941715Ethyl 3-methylthieno[2,3-c]pyridine-2-carboxylate

Produkt 1

HCID 823742933-Methylthieno[2,3-c]pyridine-2-carbaldehydeAusbeute 87 %

Reagenzien, Katalysatoren, Lösungsmittel 3

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

Versuchsvorschrift

To a mixture of ethyl 3-methylthieno[2,3-c]pyridine-2-carboxylate (2.00 g) synthesized above, calcium chloride (2.01 g), ethanol (30 mL) and tetrahydrofuran (30 mL) was added sodium borohydride (1.37 g) at 0° C., and the mixture was stirred at room temperature for 3 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 pale-yellow solid. To a solution (40 mL) of the obtained solid in tetrahydrofuran was added active manganese dioxide (8.10 g), and the mixture was stirred at 50° C. for 8 hr. Manganese dioxide was filtered off, and the filtrate was concentrated under reduced pressure to give the title object compound (1.39 g, 87%) as a pale-brown 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 pale-yellow solid
  8. stirringthe mixture was stirred at 50° C. for 8 hr
  9. filtrationManganese dioxide was filtered off
  10. concentrationthe filtrate was concentrated under reduced pressure

Quellen und Nachweise

ORD-Eintrag
ord-f86f14584d3843058d9f26a7087c7c4e
Quelldatensatz
uspto-grants-2013_05
DOI
10.6084/m9.figshare.5104873.v1
Patentnummer
US08436043B2

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