Réaction #1355648

Équation de réaction

(+/−) ethyl 4-[(5,5-dimethyl-8-hydroxy-8-carbethoxymethyl-5,6,7,8-tetrahydronaphth-2-yl)azo]benzoate

Compound D1

(+/−) ethyl 4-[(5,5-dimethyl-8-hydroxy-8-carbethoxymethyl-5,6,7,8-tetrahydronaphth-2-yl)azo]benzoate

DCC

→

title compounds

Ethyl 4-[(5,5-dimethyl-8-(carbethoxymethyl)-5,6-dihydronaphthalen-2-yl)azo]benzoate

Solvants

benzene

Conditions de réaction

Traitement

1. 1
   Températureunder reflux for 7 days
2. 2
   Filtrationthe solids were filtered out
3. 3
   Extractionthe solution was extracted with ethyl acetate
4. 4
   LavageThe combined organic layer was washed with brine
5. 5
   Séchagedried over Na2SO4
6. 6
   AutreThe solvent was removed under reduced pressure
7. 7
   Autrethe crude material was purified by flash chromatography (silicagel, 10% ethyl acetate in hexane)

Mode opératoire

A solution of (+/−) ethyl 4-[(5,5-dimethyl-8-hydroxy-8-carbethoxymethyl-5,6,7,8-tetrahydronaphth-2-yl)azo]benzoate (Compound D1, 108 mg, 0.25 mmol), DCC (55.9 mg, 0.271 mmol) and CuCl (36.6 mg, 0.37 mmol) in 8 ml of dry benzene was heated under reflux for 7 days. After cooling to room temperature, the solids were filtered out and the solution was extracted with ethyl acetate. The combined organic layer was washed with brine and dried over Na2SO4. The solvent was removed under reduced pressure, the crude material was purified by flash chromatography (silicagel, 10% ethyl acetate in hexane) to afford the pure title compounds as red oils.

Source