Reaktion #1885013

ord-4cd12ff1a290470ca8ddb4b417eecb09

Reaktionsgleichung

[Na+].[O-]Cl
Sodium hypochlorite
C1CCNCC1
piperidine
O=Cc1ccc(O)cc1O
2,4,-dihydroxybenzaldehyde
O=Cc1cc(Cl)c(O)cc1O
5-chloro-2,4-dihydroxybenzaldehyde

Lösungsmittel

Reaktionsbedingungen

Temperatur
0°CELSIUS
Detaillierte Bedingungen
See reaction.notes.procedure_details.

Aufarbeitung

  1. 1
    FiltrationAfter three additional hours, the precipitate was collected via filtration in quantitative yield
  2. 2
    SonstigeThe product can be purified via column chromatography
  3. 3
    Sonstigerecrystallizations from toluene
  4. 4
    SonstigeHowever, the 3-chloro-2,4-dihdroxybenzaldehyde does not react in the next reaction, so the product
  5. 5
    Sonstigewas used without further purification

Vorschrift

Sodium hypochlorite (75 mL, 0.055 mol) and piperidine (4.68 g, 0.055 mol) were cooled to 0° C., combined cautiously and added dropwise over 2 h to a solution of 2,4,-dihydroxybenzaldehyde (6.91 g, 0.05 mol) in 50% aqueous sulfuric acid (150 mL) while cooling to 0° C. After three additional hours, the precipitate was collected via filtration in quantitative yield. 1H NMR indicates that it is about 65% 5-chloro-2,4-dihdroxybenzaldehyde, with the balance being 3-chloro-2,4-dihdroxybenzaldehyde. The product can be purified via column chromatography and/or repeated recrystallizations from toluene. However, the 3-chloro-2,4-dihdroxybenzaldehyde does not react in the next reaction, so the product was used without further purification.

Quelle

DOI: 10.6084/m9.figshare.5104873.v1Patent: US08343710B1uspto-grants-2013_01