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ChemicalBook CAS DataBase List 2-Amino-5-hydroxypyridine
55717-46-9

2-Amino-5-hydroxypyridine synthesis

11synthesis methods
5-(benzyloxy)pyridin-2-amine

96166-00-6

2-Amino-5-hydroxypyridine

55717-46-9

The general procedure for the synthesis of 2-amino-5-hydroxypyridine from 5-(benzyloxy)pyridin-2-amine was as follows: 2-amino-5-benzyloxypyridine, ethanol (217 g) and a toluene solution (331 g) of 10% Pd/C (2.28 g, 53% moisture content) were added to an autoclave and the reaction was carried out at 25 °C. During the reaction, hydrogen was introduced into the autoclave, maintaining an absolute pressure of 0.2 MPa, and the reaction lasted for several hours. Upon completion of the reaction, the Pd/C catalyst was removed by filtration and the residue was washed with ethanol (76 g). The filtrate was dried under reduced pressure to give 2-amino-5-hydroxypyridine (25.6 g, 0.23 mol) in 92% yield.

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Yield:55717-46-9 92%

Reaction Conditions:

with palladium 10% on activated carbon;hydrogen in ethanol;toluene at 25; under 1500.15 Torr; for 4 h;Autoclave;

Steps:

4
A toluene solution (331 g) of the obtained 2-amino-5-benzyloxypyridine,Ethanol (217 g) and 10% Pd / C (2.28 g, moisture content 53%) were charged in an autoclave and reacted at 25 ° C. for 4 hours while being introduced at 0.2 MPa (absolute pressure) in a hydrogen atmosphere.After completion of the reaction, Pd / C was filtered and the residue was washed with ethanol (76 g).The filtrate was dried under reduced pressure to obtain 2-amino-5-hydroxypyridine (25.6 g, 0.23 mol) (yield 92%).

References:

KOEI CHEMICAL COMPANY LIMITED;TAKAHASHI, SATOSHI;NIHEI, YURI JP2017/48131, 2017, A Location in patent:Paragraph 0124

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