Reaktion #1331645

Reaktionsgleichung

4-nitroaniline

3,5-di-tert-butyl-4-hydroxybenzoic acid

dicyclohexylcarbodiimide

→

3,5-bis-(1,1-dimethylethyl)-4-hydroxy-N-(4-nitrophenyl)-benzamide

Ausbeute 65.0%

Lösungsmittel

THF

Reaktionsbedingungen

Aufarbeitung

1. 1
   Filtrationthe precipitate which appears is filtered out
2. 2
   Waschenrinsed with ethyl acetate
3. 3
   EinengenAfter the solution is concentrated under reduced pressure
4. 4
   workup.ADDITIONthe residue is diluted in 20 ml of ethyl acetate
5. 5
   Filtrationthe insoluble part is filtered out
6. 6
   Sonstigethe residue is precipitated from diethyl ether
7. 7
   FiltrationThe solid is recovered by filtration
8. 8
   Waschenrinsed abundantly with diethyl ether in order
9. 9
   Sonstigeto produce a white powder with a yield of 65%

Vorschrift

1.38 g (10 mmoles) of 4-nitroaniline, 2.5 g (10 mmoles) of 3,5-di-tert-butyl-4-hydroxybenzoic acid and 2.26 g (11 mmoles) of dicyclohexylcarbodiimide are introduced into a 250 ml flask containing 20 ml of THF. The reaction medium is agitated for 15 hours at ambient temperature, and the precipitate which appears is filtered out and rinsed with ethyl acetate. After the solution is concentrated under reduced pressure, the residue is diluted in 20 ml of ethyl acetate and the insoluble part is filtered out. The solvent is eliminated under vacuum and the residue is precipitated from diethyl ether. The solid is recovered by filtration, rinsed abundantly with diethyl ether in order to produce a white powder with a yield of 65%. Melting point: 277-278° C.

Quelle