Boron tribromide → Benzaldehyde, 2,3-dihydroxy-4-nitro-

HRID 2182735Notizen

Reaktionsgleichung

Reaktionsgleichung von HRID 2182735
[OH:1][C:2]1[C:9]([O:10]C)=[C:8]([N+:12]([O-:14])=[O:13])[CH:7]=[CH:6][C:3]=1[CH:4]=[O:5].B(Br)(Br)Br>ClCCl>[OH:1][C:2]1[C:9]([OH:10])=[C:8]([N+:12]([O-:14])=[O:13])[CH:7]=[CH:6][C:3]=1[CH:4]=[O:5]

Komponenten

4

Edukt 2

HCID 25134Boron tribromideHCID 149774472-Hydroxy-3-methoxy-4-nitrobenzaldehyde

Produkt 1

HCID 10442360Benzaldehyde, 2,3-dihydroxy-4-nitro-Ausbeute 95,1 %

Reagenzien, Katalysatoren, Lösungsmittel 1

HCID 6344DichloromethaneLösungsmittel

Versuchsvorschrift

17.2 g of 2-hydroxy-3-methoxy-4-nitrobenzaldehyde (J. Het. Chem. 33, (1996), 1171) in 350 ml of dichloromethane is slowly mixed at 0° C. with 175 ml of boron tribromide solution (1 M in dichloromethane), and it is stirred for another 4 hours. The batch is added to ice water, the organic phase is separated, and the aqueous phase is extracted with dichloromethane. The combined organic phases are washed with water, and the solvent is removed in a vacuum. 15.2 g of 2,3-dihydroxy-4-nitrobenzaldehyde is obtained as a red solid, flash point 122-126° C.

Aufarbeitung

  1. customthe organic phase is separated
  2. extractionthe aqueous phase is extracted with dichloromethane
  3. washThe combined organic phases are washed with water
  4. customthe solvent is removed in a vacuum

Quellen und Nachweise

ORD-Eintrag
ord-d24ac058098d43ec97c3db406218257f
Quelldatensatz
uspto-grants-2005_05
Patentnummer
US06897224B2

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