(R)-N-(3-chloroprop-1-yl)-N-(α-methyl-4'-methoxybenzyl)amine

Base Information

• Chemical Name: (R)-N-(3-chloroprop-1-yl)-N-(α-methyl-4'-methoxybenzyl)amine
• CAS No.: 1356849-85-8
• Molecular Formula: C₁₂H₁₈ClNO
• Molecular Weight: 227.734
• Mol file: 1356849-85-8.mol

Synonyms:(R)-N-(3-chloroprop-1-yl)-N-(α-methyl-4'-methoxybenzyl)amine

Chemical Property of (R)-N-(3-chloroprop-1-yl)-N-(α-methyl-4'-methoxybenzyl)amine

Chemical Property:

Purity/Quality:

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

Useful:

Technology Process of (R)-N-(3-chloroprop-1-yl)-N-(α-methyl-4'-methoxybenzyl)amine

There total 1 articles about (R)-N-(3-chloroprop-1-yl)-N-(α-methyl-4'-methoxybenzyl)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: 70.0%

1(R)-(4-methoxyphenyl)-ethylamine (6298-96-0,22038-86-4,35600-82-9,41851-59-6) + 1.3-chlorobromopropane (109-70-6) → (R)-N-(3-chloroprop-1-yl)-N-(α-methyl-4'-methoxybenzyl)amine (1356849-85-8)

Guidance literature:

DOI:10.1016/j.tetlet.2011.12.088

Reference yield: 84.0%

(R)-N-(3-chloroprop-1-yl)-N-(α-methyl-4'-methoxybenzyl)amine (1356849-85-8) + methyl cinnamate (103-26-4,1754-62-7) → methyl (3S,αR)-3-[N-( 3'-chloropropyl)-N-(α-methyl-4''-methoxybenzyl)amino]-3-phenylpropanoate (1356849-80-3)

Guidance literature:

With n-butyllithium; In tetrahydrofuran; at -78 ℃; for 2h;

DOI:10.1021/jo3012732

Reference yield:

(R)-N-(3-chloroprop-1-yl)-N-(α-methyl-4'-methoxybenzyl)amine (1356849-85-8) → (S,S)-1,4-di-[2'-oxo-4'-phenyl-N(5')-methyl-1',5'-diazocan-N(1')-yl]butane (88931-13-9,88931-14-0,20410-93-9)

Guidance literature:

Multi-step reaction with 6 steps

1.1: n-butyllithium / tetrahydrofuran / 2 h / -78 °C

2.1: sodium azide; sodium iodide / dimethyl sulfoxide / 24 h / 50 °C

3.1: triphenylphosphine / tetrahydrofuran / 0.5 h / 20 °C

3.2: 2 h / 50 °C

4.1: triethoxyantimony / toluene / 2 h / Molecular sieve; Reflux

5.1: formic acid / 2.5 h / Reflux

6.1: potassium hydroxide / dimethyl sulfoxide / 96 h / 20 °C

With n-butyllithium; sodium azide; triethoxyantimony; triphenylphosphine; sodium iodide; potassium hydroxide; In tetrahydrofuran; formic acid; dimethyl sulfoxide; toluene;

DOI:10.1021/jo3012732

upstream raw materials:

1(R)-(4-methoxyphenyl)-ethylamine

1.3-chlorobromopropane

Downstream raw materials:

methyl (3S,αR)-3-[N-( 3'-chloropropyl)-N-(α-methyl-4''-methoxybenzyl)amino]-3-phenylpropanoate

methyl (3S,αR)-3-[N-( 3'-azidopropyl)-N-(α-methyl-4''-methoxybenzyl)amino]-3-phenylpropanoate

methyl (3S,αR)-3-[N-( 3'-aminopropyl)-N-(α-methyl-4''-methoxybenzyl)amino]-3-phenylpropanoate

(4S,αR)-4-phenyl-N(5)-(α-methyl-4'-methoxybenzyl)-1,5-diazocan-2-one