HCID 12128809, Verbindung → 2,5-Dibromo-3,4-dihydro-1(2H)-naphthalenone

HRID 2308205Notizen

Reaktionsgleichung

Reaktionsgleichung von HRID 2308205
[Br:1][C:2]1(Br)[CH2:11][CH2:10][C:9]2[C:4](=[CH:5][CH:6]=[CH:7][C:8]=2[Br:12])[C:3]1=[O:13]>O>[Br:1][CH:2]1[CH2:11][CH2:10][C:9]2[C:4](=[CH:5][CH:6]=[CH:7][C:8]=2[Br:12])[C:3]1=[O:13]

Komponenten

3

Edukt 1

HCID 12128809HCID 12128809, Verbindung

Produkt 1

HCID 121288082,5-Dibromo-3,4-dihydro-1(2H)-naphthalenoneAusbeute 98,5 %

Reagenzien, Katalysatoren, Lösungsmittel 1

HCID 962WaterLösungsmittel

Versuchsvorschrift

A clear yellow solution of 5-bromo-3,4-dihydro-1(2H)-naphthalenone (12.09 g, 53.7 mmol) in freshly opened Et2O (220 mL) under an N2 atmosphere was chilled to −5° C. HCl was bubbled in subsurface for 1 min, causing no visible change. The dropwise addition of a solution of Br2 (8.58 g, 53.7 mmol) in CH2Cl2 (20 mL) and Et2O (2 mL) to the vigorously stirring solution of 5-bromo-3,4-dihydro-1(2H)-naphthalenone over 2 h (each drop was allowed to fully decolorize before adding the next) produced a product mixture that assayed by HPLC. Peak area showed 79.4% title compound, 9.5% unreacted 5-bromo-3,4-dihydro-1(2H)-naphthalenone, 0.6% unidentified, and 9.4% 2,2,5-tribromo-1-tetralone. The addition of H2O produced a top light brown organic phase, and a clear, colorless bottom aqueous phase which was separated. After drying with MgSO4, the organic layer was concentrated under vacuum at room temperature to give the crude intermediate title compound as a light brown oil (16.08 g, 98.5%).

Aufarbeitung

  1. customproduced a top light brown organic phase
  2. customa clear, colorless bottom aqueous phase which was separated
  3. dry with materialAfter drying with MgSO4
  4. concentrationthe organic layer was concentrated under vacuum at room temperature

Quellen und Nachweise

ORD-Eintrag
ord-801edc6120d447d8b22eee3494dec036
Quelldatensatz
uspto-grants-2004_12
Patentnummer
US06835733B2

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