Hydrochloric Acid → (2Z)-1-(4-bromophenyl)-2-hydroxyiminopentan-1-one

HRID 1873912Notizen

Reaktionsgleichung

Reaktionsgleichung von HRID 1873912
Cl.[Br:2][C:3]1[CH:8]=[CH:7][C:6]([C:9](=[O:14])[CH2:10][CH2:11][CH2:12][CH3:13])=[CH:5][CH:4]=1.[N:15]([O-])=[O:16].[Na+]>C1COCC1.C(OCC)C>[Br:2][C:3]1[CH:4]=[CH:5][C:6]([C:9](=[O:14])/[C:10](=[N:15]\[OH:16])/[CH2:11][CH2:12][CH3:13])=[CH:7][CH:8]=1

Komponenten

6

Edukt 3

HCID 313Hydrochloric AcidHCID 817174'-BromovalerophenoneHCID 23668193Sodium Nitrite

Produkt 1

HCID 87519930(2Z)-1-(4-bromophenyl)-2-hydroxyiminopentan-1-oneAusbeute 59,1 %

Reagenzien, Katalysatoren, Lösungsmittel 2

HCID 3283Diethyl EtherLösungsmittelHCID 8028TetrahydrofuranLösungsmittel

Versuchsvorschrift

The conc. HCl (40 mL) was added dropwise to a solution of 1-(4-bromophenyl)pentan-1-one (4.68 g, 19.41 mmol) and sodium nitrite (4.02 g, 58.2 mmol) in THF (80 ml) at 0° C. and allowed to warm to room temperature and stirred 18 hours. The reaction mixture was diluted with diethyl ether and the organic phase washed with sat'd NaHCO3 and brine. Concentration gave (Z)-1-(4-bromophenyl)-2-(hydroxyimino)pentan-1-one 3.1 g (33%) as an oil which was used without further purification.). RT=2.1 min, (Condition 1) LCMS: Anal. Calcd. for C11H12BrN1O2 270.01. found: 270.15 (M+H)+.

Aufarbeitung

  1. washthe organic phase washed with sat'd NaHCO3 and brine
  2. concentrationConcentration

Quellen und Nachweise

ORD-Eintrag
ord-4901a9bc8e0e45128a7b2683e10d12e2
Quelldatensatz
uspto-grants-2012_11
Patentnummer
US08303944B2

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