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Phosphorus oxychloride → 4-chloro-5H,6H,7H-cyclopenta[b]pyridine

HRID 924397
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Druckvorschau

Reaktionsgleichung

Reaktionsgleichung von HRID 924397
[N+:1]1([O-])[CH:6]=[CH:5][CH:4]=[C:3]2[CH2:7][CH2:8][CH2:9][C:2]=12.P(Cl)(Cl)([Cl:13])=O>>[Cl:13][C:4]1[CH:5]=[CH:6][N:1]=[C:2]2[CH2:9][CH2:8][CH2:7][C:3]=12
KomponentenReaktionsbedingungenVersuchsvorschriftAufarbeitungQuellen und NachweiseNotizen zur Reaktion

Komponenten

3

Edukt 2

HCID 24813Phosphorus oxychlorideHCID 131533156,7-Dihydro-5H-cyclopenta[b]pyridine 1-oxide

Produkt 1

HCID 122033274-chloro-5H,6H,7H-cyclopenta[b]pyridineAusbeute 94 %

Reaktionsbedingungen

Temperatur
120 °C

Versuchsvorschrift

6,7-Dihydro-5H-cyclopenta[b]pyridine 1-oxide (2.5 g, 18 mmol) was mixed with phosphoryl chloride (20 mL, 200 mmol). The reaction mixture was stirred at 120° C. for 3 h. The excess POCl3 was removed under reduced pressure. The residue was diluted in 80 mL of EtOAc and neutralized with Na2CO3 solution. After filtration, the aqueous layer was extracted with EtOAc twice. The combined organic extracts were dried, filtered and concentrated under reduced pressure to give the sub-title compound (2.6 g, 93%). LCMS calc. for C8H9ClN (M+H)+: m/z=154.2. Found: 154.3.

Aufarbeitung

  1. customThe excess POCl3 was removed under reduced pressure
  2. additionThe residue was diluted in 80 mL of EtOAc and neutralized with Na2CO3 solution
  3. filtrationAfter filtration
  4. extractionthe aqueous layer was extracted with EtOAc twice
  5. customThe combined organic extracts were dried
  6. filtrationfiltered
  7. concentrationconcentrated under reduced pressure

Quellen und Nachweise

ORD-Eintrag
ord-5dd0709017394eb7a3f7935c286067bf
Quelldatensatz
uspto-grants-2016_03
DOI
10.6084/m9.figshare.5104873.v1
Patentnummer
US09278950B2

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