StartseiteMCPWorkbenchSkills
StartseiteWorkbenchBenachrichtigungenMein Bereich
llms.txt · MCP-AnleitungDatenschutz · Nutzungsbedingungen · Supportv1.8.0
  1. Startseite
  2. /Reaktion

Chlorosuccinimide → 1-Chloro-3-methylnaphthalen-2-ol

HRID 513999
Notizen
Druckvorschau

Reaktionsgleichung

Reaktionsgleichung von HRID 513999
[Cl:1]N1C(=O)CCC1=O.[CH3:9][C:10]1[C:11]([OH:20])=[CH:12][C:13]2[C:18]([CH:19]=1)=[CH:17][CH:16]=[CH:15][CH:14]=2>ClCCl.[Cl-].[Zr+4].[Cl-].[Cl-].[Cl-]>[Cl:1][C:12]1[C:13]2[C:18](=[CH:17][CH:16]=[CH:15][CH:14]=2)[CH:19]=[C:10]([CH3:9])[C:11]=1[OH:20]
KomponentenReaktionsbedingungenVersuchsvorschriftAufarbeitungQuellen und NachweiseNotizen zur Reaktion

Komponenten

5

Edukt 2

HCID 31398ChlorosuccinimideHCID 870503-Methyl-2-naphthol

Produkt 1

HCID 671260841-Chloro-3-methylnaphthalen-2-olAusbeute 78,2 %

Reagenzien, Katalysatoren, Lösungsmittel 2

HCID 9856075Zirconium chloride (ZrCl4), (T-4)-KatalysatorHCID 6344DichloromethaneLösungsmittel

Reaktionsbedingungen

Temperatur
-78 °C

Versuchsvorschrift

To a solution of N-chlorosuccinimide (8.02 g, 60.05 mmol) in dichloromethane (475 mL) at −78° C. was added zirconium(IV)chloride (2.80 g, 12.01 mmol), followed by 3-methyl-naphthalen-2-ol (4A) (9.5 g, 60.05 mmol) under Ar. The reaction mixture was stirred at −78° C. for minutes, the cooling bath was removed and the reaction was stirred at room temperature for 5 h. The reaction was quenched with saturated sodium bicarbonate solution and stirred for 5 minutes. The mixture was diluted with H2O, extracted with dichloromethane (3×) and the combined organic layer was dried (MgSO4), filtered, concentrated and purified by flash column chromatography (silica gel, 0 to 10% ethyl acetate/hexanes) to give 4B as a white solid (9.05 g, 78%).

Aufarbeitung

  1. customthe cooling bath was removed
  2. stirringthe reaction was stirred at room temperature for 5 h
  3. customThe reaction was quenched with saturated sodium bicarbonate solution
  4. stirringstirred for 5 minutes
  5. additionThe mixture was diluted with H2O
  6. extractionextracted with dichloromethane (3×)
  7. dry with materialthe combined organic layer was dried (MgSO4)
  8. filtrationfiltered
  9. concentrationconcentrated
  10. custompurified by flash column chromatography (silica gel, 0 to 10% ethyl acetate/hexanes)

Quellen und Nachweise

ORD-Eintrag
ord-435ecd70b6fc457bba605152cc2fc458
Quelldatensatz
uspto-grants-2015_08
DOI
10.6084/m9.figshare.5104873.v1
Patentnummer
US09102614B2

Notizen zur Reaktion

Wird geladen…

Auf dieser SeiteKomponentenReaktionsbedingungenVersuchsvorschriftAufarbeitungQuellen und NachweiseNotizen zur Reaktion