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1750-79-4

4-(5-amino-1,3,4-oxadiazol-2-yl)phenol(SALTDATA: FREE) synthesis

4synthesis methods
-

Yield: 93%

Reaction Conditions:

with pyridine;manganese(IV) oxide at 120;Green chemistry;

Steps:

13 2-amino-5-(4'-hydroxyphenyl)-1,3,4-oxadiazole
To a dry threeneckedflask Amol 2(4'hydroxyphenyl)methylene semicarbazide, Bmol CmL manganese dioxide andpyridine at 120 ° C under stirring reaction, the reaction was monitored by TLC reaction Until aminals urea feed pointdisappears, to obtain a reaction mixture wherein, A: B: C = 1: 1.1: 8 TLC monitoring When measuring the eluent used is amixture of ethyl acetate and petroleum ether made, and ethyl acetate and petroleum ether The volume ratio of 1: 5[2]2)The reaction mixture was cooled to room temperature, vacuum filtration, and the filtrate was concentrated to dryness togive, as a white solid Body, a white solid was washed with water, vacuum filtration to give the crude product, the crudeproduct was recrystallized from anhydrous ethanol 2Amino5(4'hydroxyphenyl)1,3,4oxadiazolepure, yield of 93%.

References:

Shaanxi University of Science and Technology;YIN, DA WEI;ZHANG, XIAO LI;LIU, SEN;QIAO, SEN;ZHAO, BIN JIE;YANG, AN NING;WANG, JIN YU;LU, BO CN103980222, 2016, B Location in patent:Paragraph 0065-0067