Réaction #482823

Équation de réaction

4-(4-chlorophenyl)-2-(2-methyl-1-imidazolyl)-5-oxazolepropanol

5,5,8,8-tetramethyl-5,6,7,8-tetrahydro-2-naphthalenol

tributylphosphine

1,1′-(azodicarbonyl)dipiperidine

→

4-(4-chlorophenyl)-2-(2-methyl-1-imidazolyl)-5-[3-(5,5,8,8-tetramethyl-5,6,7,8-tetrahydro-2-naphthalenyloxy)propyl]oxazole

Solvants

tetrahydrofuran

Conditions de réaction

Traitement

1. 1
   ConcentrationAfter the reaction mixture was concentrated

Mode opératoire

To a mixture of 4-(4-chlorophenyl)-2-(2-methyl-1-imidazolyl)-5-oxazolepropanol (318 mg), 5,5,8,8-tetramethyl-5,6,7,8-tetrahydro-2-naphthalenol (409 mg), tributylphosphine (405 mg) and tetrahydrofuran (10 ml) was added 1,1′-(azodicarbonyl)dipiperidine (500 mg) at room temperature, and the resulting mixture was stirred for 1 hour. After the reaction mixture was concentrated, the residue was subjected to silica gel column chromatography, and 4-(4-chlorophenyl)-2-(2-methyl-1-imidazolyl)-5-[3-(5,5,8,8-tetramethyl-5,6,7,8-tetrahydro-2-naphthalenyloxy)propyl]oxazole was obtained as a yellow oil (400 mg, 79%) from an ethyl acetate-hexane (1:1, v/v)-eluted fraction.

Source