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Methane → HCID 178524700, Verbindung

HRID 1013623
Notizen
Druckvorschau

Reaktionsgleichung

Reaktionsgleichung von HRID 1013623
[Br:1][C:2]1[CH:11]=[C:10]2[C:5]([C:6](=[O:17])[C:7]([C:12]([O:14]CC)=[O:13])=[CH:8][NH:9]2)=[N:4][CH:3]=1.[OH-].[Na+].C>O>[Br:1][C:2]1[CH:11]=[C:10]2[C:5]([C:6]([OH:17])=[C:7]([C:12]([OH:14])=[O:13])[CH:8]=[N:9]2)=[N:4][CH:3]=1
KomponentenVersuchsvorschriftAufarbeitungQuellen und NachweiseNotizen zur Reaktion

Komponenten

5

Edukt 3

HCID 297MethaneHCID 14798Sodium HydroxideHCID 13459134Ethyl 7-bromo-4-oxo-1,4-dihydro-1,5-naphthyridine-3-carboxylate

Produkt 1

HCID 178524700HCID 178524700, Verbindung

Reagenzien, Katalysatoren, Lösungsmittel 1

HCID 962WaterLösungsmittel

Versuchsvorschrift

Ethyl 7-bromo-4-oxo-1,4-dihydro-1,5-naphtyridine-3-carboxylate (1 g, 3 mmol) and 2.5 M NaOH (10 mL) were refluxed for 1 h in a RBF fitted with a reflux condenser. The hot, heterogeneous mixture was diluted with boiling water at which point a tan precipitate dissolved. Charcoal was added to the solution, which was swirled for 2 min and then the mixture was filtered. Glacial acetic acid was added to the filtrate and a white precipitate started to form (pH adjusted to 4). The precipitate was filtered off upon cooling, washed with water and dried to provide the desired product as a white solid.

Aufarbeitung

  1. customfitted with a reflux condenser
  2. dissolutiondissolved
  3. filtrationthe mixture was filtered
  4. additionGlacial acetic acid was added to the filtrate
  5. customto form (pH adjusted to 4)
  6. filtrationThe precipitate was filtered off
  7. temperatureupon cooling
  8. washwashed with water
  9. customdried

Quellen und Nachweise

ORD-Eintrag
ord-699020fbf3184c7c93c646ee7b0205ff
Quelldatensatz
uspto-grants-2011_07
DOI
10.6084/m9.figshare.5104873.v1
Patentnummer
US07981891B2

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