Hydrochloric Acid → 6-Bromo-2-naphthalenol

HRID 725695

Reaktionsgleichung

Reaktionsgleichung von HRID 725695
C(O)C.Cl.[Sn].Br[C:7]1[C:16]2[C:11](=[CH:12][C:13]([Br:17])=[CH:14][CH:15]=2)[CH:10]=[CH:9][C:8]=1[OH:18]>C1C=CC=CC=1.C(OCC)(=O)C>[Br:17][C:13]1[CH:12]=[C:11]2[C:16](=[CH:15][CH:14]=1)[CH:7]=[C:8]([OH:18])[CH:9]=[CH:10]2

Komponenten

6

Edukt 4

HCID 313Hydrochloric AcidHCID 702EthanolHCID 277682-Naphthol, 1,6-dibromo-HCID 5352426Tin atom

Produkt 1

HCID 271446-Bromo-2-naphthalenolAusbeute 103,1 %

Reagenzien, Katalysatoren, Lösungsmittel 1

HCID 21583983Benzene ethyl acetateLösungsmittel

Versuchsvorschrift

To a solution of 225 mL of ethanol and 90 mL of conc. HCl in a 500 mL round bottom flask were added of tin metal (32.6 g, 274 mmol) and 1,6-dibromo-2-naphthol (41.5 g, 137 mmol). The reaction mixture was refluxed on a steam bath for 9 hours. TLC (SiO2, 15:1 benzene/ethyl acetate) indicated consumption of starting material. The cooled solution was decanted from unreacted tin, concentrated to 150-200 mL on vacuo and poured into 600 mL of ice and water. The white precipitate was collected on a Buchner funnel and dried in the air to afford 31.5 g of an off-white solid. Recrystallization from benzene produced 23.8 g of pure product (78%): mp 127°-127.5° C.; lit. mp 127°-129° C.; reference: C. R. Koelsch, Org. Syn. Coll. Vol. 3, 132 (1955). ##STR25##

Aufarbeitung

  1. temperatureThe reaction mixture was refluxed on a steam bath for 9 hours
  2. customconsumption of starting material
  3. customThe cooled solution was decanted from unreacted tin
  4. concentrationconcentrated to 150-200 mL on vacuo
  5. additionpoured into 600 mL of ice and water
  6. customThe white precipitate was collected on a Buchner funnel
  7. customdried in the air

Quellen und Nachweise

ORD-Eintrag
ord-b6104a1a69a842ab8eb22aaefe61fb4e
Quelldatensatz
uspto-grants-1998_01
Patentnummer
US05707559

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