Réaction #410330

ord-5a15c12ba5824e078d19a9fdc2ba8f51

Équation de réaction

CCOCC
diethyl ether
Cc1ccc(-c2ccccc2C(=O)Nc2ccc(C(=O)N(C)c3ccccc3CO)cc2)cc1
4-(4′-methylbiphenyl-2-carboxamido)-N-methyl-N-(2-hydroxymethylphenyl)benzamide
[Mg+2].[O-][O-]
magnesium dioxide
CO
methanol
Cc1ccc(-c2ccccc2C(=O)Nc2ccc(C(=O)N(C)c3ccccc3C=O)cc2)cc1
4-(4′-methylbiphenyl-2-carboxamido)-N-methyl-N-(2-formylphenyl)benzamide
Rendement 93.3%

Conditions de réaction

Conditions détaillées
See reaction.notes.procedure_details.

Traitement

  1. 1
    Températurewas refluxed for 3 hours
  2. 2
    Filtrationthe solution was filtered through Celite
  3. 3
    AutreThe filtrate was evaporated in vacuo
  4. 4
    Autreto give a crude oil

Mode opératoire

A mixture of 4-(4′-methylbiphenyl-2-carboxamido)-N-methyl-N-(2-hydroxymethylphenyl)benzamide (225 mg) and magnesium dioxide (651 mg) in chloroform (10 ml) was refluxed for 3 hours and the solution was filtered through Celite. The filtrate was evaporated in vacuo to give a crude oil and the oil was subjected to silica gel column (1% methanol in chloroform). The product was solidified with diethyl ether to give 4-(4′-methylbiphenyl-2-carboxamido)-N-methyl-N-(2-formylphenyl)benzamide (209 mg) as a white powder.

Source

DOI: 10.6084/m9.figshare.5104873.v1Brevet: US06211242B1uspto-grants-2001_04