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2-Chloro-6-methylaniline → 7-chloro-1H-indazole

HRID 334638
Notizen
Druckvorschau

Reaktionsgleichung

Reaktionsgleichung von HRID 334638
[Cl:1][C:2]1[CH:7]=[CH:6][CH:5]=[C:4]([CH3:8])[C:3]=1[NH2:9].[N:10]([O-])=O.[Na+].C([O-])(=O)C.[Na+]>OS(O)(=O)=O.O>[Cl:1][C:2]1[CH:7]=[CH:6][CH:5]=[C:4]2[C:3]=1[NH:9][N:10]=[CH:8]2
KomponentenReaktionsbedingungenVersuchsvorschriftAufarbeitungQuellen und NachweiseNotizen zur Reaktion

Komponenten

6

Edukt 3

HCID 68972-Chloro-6-methylanilineHCID 517045Sodium AcetateHCID 23668193Sodium Nitrite

Produkt 1

HCID 111162497-chloro-1H-indazoleAusbeute 41 %

Reagenzien, Katalysatoren, Lösungsmittel 2

HCID 962WaterLösungsmittel3×HCID 1118
Sulfuric Acid
Lösungsmittel

Reaktionsbedingungen

Temperatur
7.5 °C

Versuchsvorschrift

A solution of 2-chloro-6-methyl-phenylamine (500 mg, 3.53 mmol) in H2SO4 (1.37 mL) was diluted by adding over 15 min. 2 mL of water in order to maintain a temperature below 90° C. Then the reaction mixture was cooled to 5-10° C. and a solution of sodium nitrite (246 mg, 3.57 mmol) in water (1 mL) was added over 2 hours. The resulting diazonium solution was then added to a solution of sodium acetate (5.21 g, 63.6 mmol) in water (20 mL) at a temperature maintained between 65 to 75° C. The resulting precipitate was filtered and treated with a solution of NaOH (6.00 g) in water (100 mL) at 95-100° C. The aqueous phase was separated while hot from the small amount of black tarry by-products, cooled to 50-60° C. and acidified with HCl (37%, 12.5 mL). The reaction mixture was cooled down to room temperature, the resulting precipitate was filtered, was washed thrice with cold water and was dried under vacuum to yield 7-chloro-1H-indazole (220 mg, 1.44 mmol, 41%) as a white solid.

Aufarbeitung

  1. additionby adding over 15 min
  2. temperaturemaintained between 65 to 75° C
  3. filtrationThe resulting precipitate was filtered
  4. additiontreated with a solution of NaOH (6.00 g) in water (100 mL) at 95-100° C
  5. customThe aqueous phase was separated while hot from the small amount of black tarry by-products
  6. temperaturecooled to 50-60° C.
  7. temperatureThe reaction mixture was cooled down to room temperature
  8. filtrationthe resulting precipitate was filtered
  9. washwas washed thrice with cold water
  10. customwas dried under vacuum

Quellen und Nachweise

ORD-Eintrag
ord-c8ae5b2e49c64cb1bd87c65406178cfa
Quelldatensatz
uspto-grants-2014_11
DOI
10.6084/m9.figshare.5104873.v1
Patentnummer
US08883826B2

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