314768-38-2

Upstream product

• 885674-30-6 2-methyl-3-(3,4-dimethoxyphenyl)-4-phenyl-[1,2,4]oxadiazolin-5-one 
• 120-14-9 3,4-dimethoxy-benzaldehyde 
• 4229-44-1 N-methylhydroxyamine hydrochloride 
• 63-64-9 N-methylveratrylamine 

Downstream Products

• 2169-98-4 3,4-Dimethoxy-benzaldehyde oxime 
• 4229-44-1 N-methylhydroxyamine hydrochloride 
• 885674-30-6 2-methyl-3-(3,4-dimethoxyphenyl)-4-phenyl-[1,2,4]oxadiazolin-5-one 
• 27895-67-6 N-(3,4-dimethoxybenzylidene)aniline 
• 1037455-24-5 3-(3,4-dimethoxyphenyl)-2-methyl-5-trichloromethyl-Δ⁴-1,2,4-oxadiazoline 
• 1037455-46-1 (Z)-N-(3,4-dimethoxyphenyl)-N-methyl-N'-(trichloroacetyl)-formamidine 

Relevant academic research and scientific papers

Synthesis of 5-trichloromethyl-Δ4-1,2,4-oxadiazolines and their rearrangement into formamidine derivatives

A series of 5-trichloro-Δ4-1,2,4-oxadiazolines have been synthesised by 1,3-dipolar cycloaddition of nitrones to trichloroacetonitrile. These oxadiazolines rearrange into formamidine derivatives, via ring opening and a 1,2-aryl shift from carbo

Cycloaddition of acyclic nitrones with phenyl isocyanate: Synthesis and ring-opening reactions of 1,2,4-oxadiazolidin-5-ones

The cycloaddition of nitrones with unsubstituted or electron-donating substituents on the C-phenyl 1a,c,f with phenyl isocyanate proceeds smoothly for a short time with high yields to give the corresponding 1,2,4-oxadiazolidinone 2, and 1b,d,e with electron-withdrawing substituents gave the corresponding oxadiazolidinone in moderate yields after prolonged heating. Oxadiazolidinones 2a,c,f undergo diethylamine-induced fragmentation for a short time to give the corresponding Schiff bases, and oxadiazolidinones 2b,d,e remain unchanged in these conditions. Prolonged heating of 2d,e in the presence of diethylamine led to complex mixtures. In the case of 2b the corresponding amidine was the main product of the reaction. Copyright Taylor & Francis Group, LLC.

One-pot synthesis and hydroxylaminolysis of asymmetrical acyclic nitrones

Aromatic aldehydes 1 were reductively aminated to the corresponding secondary amines 2 using NaBH4 in methanol in good yields. Amines 2 were oxidized with H2O2-WO42- regioselectively to nitrones 3, the structures of which were easily determined by reacting them with hydroxylamine hydrochloride as well as by spectral means. The products of hydroxylaminolysis in ether proved to be the corresponding benzaldehyde oximes 4 and benzyl or methyl hydroxylamine hydrochlorides 5. Copyright Taylor & Francis, Inc.