(2S,4aS,7R,8aR)-[2-(N-benzyl-4,4,7-trimethyl-octahydrobenzo[e][1,3]oxazin-2-yl)benzylidene]-(4-methoxyphenyl) amine

Base Information

• Chemical Name: (2S,4aS,7R,8aR)-[2-(N-benzyl-4,4,7-trimethyl-octahydrobenzo[e][1,3]oxazin-2-yl)benzylidene]-(4-methoxyphenyl) amine
• CAS No.: 865262-78-8
• Molecular Formula: C₃₂H₃₈N₂O₂
• Molecular Weight: 482.666

Synonyms:(2S,4aS,7R,8aR)-[2-(N-benzyl-4,4,7-trimethyl-octahydrobenzo[e][1,3]oxazin-2-yl)benzylidene]-(4-methoxyphenyl) amine

Chemical Property of (2S,4aS,7R,8aR)-[2-(N-benzyl-4,4,7-trimethyl-octahydrobenzo[e][1,3]oxazin-2-yl)benzylidene]-(4-methoxyphenyl) amine

Chemical Property:

Purity/Quality:

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

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Technology Process of (2S,4aS,7R,8aR)-[2-(N-benzyl-4,4,7-trimethyl-octahydrobenzo[e][1,3]oxazin-2-yl)benzylidene]-(4-methoxyphenyl) amine

There total 3 articles about (2S,4aS,7R,8aR)-[2-(N-benzyl-4,4,7-trimethyl-octahydrobenzo[e][1,3]oxazin-2-yl)benzylidene]-(4-methoxyphenyl) amine 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: 98.0%

(2S,4aS,7R,8aR)-N-benzyl-2-(o-formylphenyl)-4,4,7-trimethyl-octahydrobenzo[e][1,3]oxazine (865262-74-4) + 4-methoxy-aniline (104-94-9) → (2S,4aS,7R,8aR)-[2-(N-benzyl-4,4,7-trimethyl-octahydrobenzo[e][1,3]oxazin-2-yl)benzylidene]-(4-methoxyphenyl) amine (865262-78-8)

Guidance literature:

In dichloromethane; at 20 ℃;

DOI:10.1021/jo0509509

Reference yield:

(1R,2S,5R)-5-methyl-2-<1-methyl-1-(benzylamino)ethyl>cyclohexan-1-ol (115156-56-4) → (2S,4aS,7R,8aR)-[2-(N-benzyl-4,4,7-trimethyl-octahydrobenzo[e][1,3]oxazin-2-yl)benzylidene]-(4-methoxyphenyl) amine (865262-78-8)

Guidance literature:

Multi-step reaction with 2 steps

1: 90 percent / benzene / 16 h / Heating

2: 98 percent / CH₂Cl₂ / 20 °C

In dichloromethane; benzene;

DOI:10.1021/jo0509509

Reference yield:

o-phthalic dicarboxaldehyde (643-79-8) → (2S,4aS,7R,8aR)-[2-(N-benzyl-4,4,7-trimethyl-octahydrobenzo[e][1,3]oxazin-2-yl)benzylidene]-(4-methoxyphenyl) amine (865262-78-8)

Guidance literature:

Multi-step reaction with 2 steps

1: 90 percent / benzene / 16 h / Heating

2: 98 percent / CH₂Cl₂ / 20 °C

In dichloromethane; benzene;

DOI:10.1021/jo0509509

upstream raw materials:

(2S,4aS,7R,8aR)-N-benzyl-2-(o-formylphenyl)-4,4,7-trimethyl-octahydrobenzo[e][1,3]oxazine

4-methoxy-aniline

(1R,2S,5R)-5-methyl-2-<1-methyl-1-(benzylamino)ethyl>cyclohexan-1-ol

o-phthalic dicarboxaldehyde

Downstream raw materials:

(2S,2'S,4a'S,7'R,8a'R)-{[2-(N-benzyl-4',4',7'-trimethyl-octahydrobenzo[e][1,3]oxazin-2'-yl)phenyl]furan-2-yl-methyl}-(4-methoxyphenyl) amine

(1R,2S,5S,7S)-2-[3-(4-methoxyphenyl)-4-oxo-10-oxa-3-azatricyclo[5.2.1.0^1,5]dec-2-yl]benzaldehyde

(1R,2S,5S,6S,7S)-2-[6-methyl-3-(4-methoxyphenyl)-4-oxo-10-oxa-3-azatricyclo[5.2.1.0^1,5]dec-2-yl]benzaldehyde

(1R,2S,5S,7S)-2-[5-methyl-3-(4-methoxyphenyl)-4-oxo-10-oxa-3-azatricyclo[5.2.1.0^1,5]dec-2-yl]benzaldehyde

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