Reaktion #51206

ord-967ddfe73b30491d9915c6116112b85f

Reaktionsgleichung

Cl
HCl
C=O
paraformaldehyde
Cc1cccc(O)c1
3-methyl-phenol
[Cl][Sn]([Cl])([Cl])[Cl]
SnCl4
Cc1ccc(C=O)c(O)c1
title product
Ausbeute 25.5%
Cc1ccc(C=O)c(O)c1
2-Hydroxy-4-methyl-benzaldehyde
Ausbeute 25.5%

Lösungsmittel

Reaktionsbedingungen

Temperatur
100°CELSIUS
Detaillierte Bedingungen
See reaction.notes.procedure_details.

Aufarbeitung

  1. 1
    ExtraktionThe solution was extracted with ether (25 ml)
  2. 2
    Waschenwashed with brine (20 ml)
  3. 3
    Trocknendried (MgSO4)
  4. 4
    Filtrationfiltered
  5. 5
    Sonstigeevaporated to a brown oil
  6. 6
    SonstigeThis oil was purified by column chromatography

Vorschrift

To a stirred solution of 3-methyl-phenol (1 g, 9.2 mmol) in toluene (5 ml) at room temperature under nitrogen was added SnCl4 (241 mg, 0.92 mmol) and tri-nbutylamine (0.6 ml, 2.77 mmol). After 20 min, paraformaldehyde (611 mg, 20.3 mmol) was added and the whole stirred at 100° C. for 16 h. The reaction mixture was diluted with water (20 ml) and acidified with 2N HCl to pH2. The solution was extracted with ether (25 ml), washed with brine (20 ml), dried (MgSO4) filtered and evaporated to a brown oil. This oil was purified by column chromatography using 5% EtOAc in pentane as eluant to provide the title product (319 mg, 25%); 1HNMR (400 MHz, CDCl3) δ: 2.3 (s, 3H), 6.75 (m, 2H), 7.35 (d, 1H), 9.75 (s, 1H), 11.00 (s, 1H).

Quelle

DOI: 10.6084/m9.figshare.5104873.v1Patent: US06849649B2uspto-grants-2005_02