13313-17-2

Upstream product

• 95-55-6 2-amino-phenol 
• 104-88-1 4-chlorobenzaldehyde 
• 117909-29-2 N-4-chlorobenzylidene-2-hydroxyaniline 

Downstream Products

• 1402042-61-8 4-(4-chlorobenzyl)-2,2-dimethyl-2H-benzo[b][1,4]oxazin-3(4H)-one 
• 385797-62-6 4-(4-chlorobenzyl)-2H-benzo[b][1,4]oxazin-3(4H)-one 
• 688761-01-5 4-(4-chlorobenzyl)-2-ethyl-2H-benzo[b][1,4]oxazin-3(4H)-one 

Relevant academic research and scientific papers

Selective alkylation of aminophenols

O-or N-Alkylated derivatives of aminophenols are important synthetic intermediates in organic synthesis. A series of aminophenols were selectively alkylated on their hydroxyl group in good yields via benzaldehyde protection of the amino group, subsequent alkylation, and hydrolysis; or on their amino group via imination and following reduction. ARKAT USA, Inc.

Sodium borohydride on wet clay: Solvent-free reductive amination of carbonyl compounds using microwaves

A solvent-flee reductive amination of carbonyl compounds by wet montmorillonite K 10 clay supported sodium borohydride is described; microwave irradiation facilitates the procedure.