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89702-89-6

3-Hydroxy-4-methoxy benzylamine synthesis

3synthesis methods
52805-46-6 Synthesis
3-Hydroxy-4-methoxybenzonitrile

52805-46-6
194 suppliers
$6.00/1g

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Yield:89702-89-6 90%

Reaction Conditions:

with sodium tetrahydroborate;copper ferrite in water; for 0.166667 h;Reflux;Green chemistry;chemoselective reaction;

Steps:

General procedure for the reduction of nitriles to primary amines

General procedure: As a representative example, in a round-bottom flask (15 mL) equipped with a magnetic stirrer, benzonitrile (1 mmol, 0.103 g) was dissolved in H2O (2 mL). Afterward, CuFe2O4 (0.2 mmol, 0.048 g) was added and the mixture was stirred. Then, NaBH4 (2 mmol, 0.076 g) was also added, and the resulting mixture continued to stir at reflux for 5 min. Upon completion of the reaction (monitored by TLC), the mixture was cooled to room temperature, and the catalyst was separated by an external magnet. The reaction mixture was extracted with ethyl acetate (EtOAc) (2 x 4 mL). The organic layers were combined together and dried over anhydrous sodium sulfate (Na2SO4). The solvent was evaporated under reduced pressure. The pure colorless liquid benzylamine was obtained in 95% yield.

References:

Zeynizadeh, Behzad;Mohammad Aminzadeh, Farkhondeh;Mousavi, Hossein [Research on Chemical Intermediates,2019]

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