2-Naphthalenamine, N-[(3,4-dimethoxyphenyl)methyl]-

Base Information

• Chemical Name: 2-Naphthalenamine, N-[(3,4-dimethoxyphenyl)methyl]-
• CAS No.: 65958-18-1
• Molecular Formula: C₁₉H₁₉NO₂
• Molecular Weight: 293.365
• DSSTox Substance ID: DTXSID30358460
• Wikidata: Q82139045

Synonyms:2-Naphthalenamine, N-[(3,4-dimethoxyphenyl)methyl]-;65958-18-1;N-[(3,4-dimethoxyphenyl)methyl]naphthalen-2-amine;DTXSID30358460

Chemical Property of 2-Naphthalenamine, N-[(3,4-dimethoxyphenyl)methyl]-

Chemical Property:

• XLogP3: 4.6
• Hydrogen Bond Donor Count: 1
• Hydrogen Bond Acceptor Count: 3
• Rotatable Bond Count: 5
• Exact Mass: 293.141578849
• Heavy Atom Count: 22
• Complexity: 335

Purity/Quality:

99% ^*data from raw suppliers

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

SDS file from LookChem

Useful:

• Canonical SMILES: COC1=C(C=C(C=C1)CNC2=CC3=CC=CC=C3C=C2)OC

Technology Process of 2-Naphthalenamine, N-[(3,4-dimethoxyphenyl)methyl]-

There total 7 articles about 2-Naphthalenamine, N-[(3,4-dimethoxyphenyl)methyl]- which guide to synthetic route it. The literature collected by LookChem mainly comes from the sharing of users and the free literature resources found by Internet computing technology. We keep the original model of the professional version of literature to make it easier and faster for users to retrieve and use. At the same time, we analyze and calculate the most feasible synthesis route with the highest yield for your reference as below:

synthetic route:

Reference yield: 49.0%

[1-(3,4-Dimethoxy-phenyl)-meth-(E)-ylidene]-naphthalen-2-yl-amine → N-(3,4-Dimethoxybenzyl)-β-naphthylamin (65958-18-1)

Guidance literature:

With sodium tetrahydroborate; acetic acid; In benzene; Reflux;

DOI:10.1134/S1070428012110085

Reference yield: 29.0%

3,4-dimethoxy-benzaldehyde (120-14-9) + 1-methylcyclohexan-4-one (589-92-4) + naphthalen-2-ylamine (91-59-8) → N-(3,4-Dimethoxybenzyl)-β-naphthylamin (65958-18-1) + 5-(3,4-dimethoxy-phenyl)-3-methyl-1,2,3,4-tetrahydro-benzo[a]phenanthridine

Guidance literature:

With hydrogenchloride; In ethanol; Heating;

DOI:10.1023/B:RUJO.0000036073.49961.28

Reference yield: 23.0%

3,4-dimethoxy-benzaldehyde (120-14-9) + naphthalen-2-ylamine (91-59-8) + 3-Methylcyclohexanone (591-24-2,625-96-7) → N-(3,4-Dimethoxybenzyl)-β-naphthylamin (65958-18-1) + 5-(3,4-dimethoxy-phenyl)-2-methyl-1,2,3,4-tetrahydro-benzo[a]phenanthridine

Guidance literature:

With hydrogenchloride; In ethanol; Heating;

DOI:10.1023/B:RUJO.0000036073.49961.28

upstream raw materials:

3,4-dimethoxy-benzaldehyde

1-methylcyclohexan-4-one

naphthalen-2-ylamine

3-Methylcyclohexanone

Downstream raw materials:

4-(3,4-dimethoxybenzyl)-1,4-dihydro-3H-spiro[benzo[f]quinoline-2,1'-cyclohexane]2',6'-dione

4-(3,4-dimethoxybenzyl)-4',4'dimethyl-1,4-dihydro-3H-spiro[benzo[f]quinoline-2,1'-cyclohexane]2',6'-dione

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