2-[(2-Methoxy-benzyl)-Methyl-aMino]-ethanol

Base Information

• Chemical Name: 2-[(2-Methoxy-benzyl)-Methyl-aMino]-ethanol
• CAS No.: 100054-98-6
• Molecular Formula: C11H17NO2
• Molecular Weight: 195.25800
• Mol file: 100054-98-6.mol

Synonyms:N-(2-methoxybenzyl)-N-methylethanolamine;2-[(2-Methoxy-benzyl)-methyl-amino]-aethanol;2-[(2-methoxy-benzyl)-methyl-amino]-ethanol;

Chemical Property of 2-[(2-Methoxy-benzyl)-Methyl-aMino]-ethanol

Chemical Property:

• Boiling Point: 102 - 105 °C (0.2 mmHg)
• PSA: 32.70000
• LogP: 1.11930

Purity/Quality:

2-((2-Methoxybenzyl)(methyl)amino)ethanol 97% ^*data from reagent suppliers

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

SDS file from LookChem

Useful:

Technology Process of 2-[(2-Methoxy-benzyl)-Methyl-aMino]-ethanol

There total 4 articles about 2-[(2-Methoxy-benzyl)-Methyl-aMino]-ethanol 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: 86.0%

formaldehyd (50-00-0,30525-89-4,61233-19-0) + N-(2-hydroxyethyl)-N-(2-methoxylbenzyl)amine (109926-15-0) → N-(2-hydroxyethyl)-N-(2-methoxylbenzyl)methylamine (100054-98-6)

Guidance literature:

With formic acid; In water; at 100 ℃; for 2h;

DOI:10.1016/j.tetasy.2009.10.025

Reference yield:

2-(2-Methoxy-phenyl)-3-methyl-oxazolidine (67625-14-3) → N-(2-hydroxyethyl)-N-(2-methoxylbenzyl)methylamine (100054-98-6)

Guidance literature:

With potassium; In tetrahydrofuran; for 24h; Yield given; Ambient temperature;

DOI:10.1021/jo00076a033

Reference yield:

ortho-anisaldehyde (135-02-4) → N-(2-hydroxyethyl)-N-(2-methoxylbenzyl)methylamine (100054-98-6)

Guidance literature:

Multi-step reaction with 2 steps

1: NH₄Cl / benzene / Heating

2: K / tetrahydrofuran / 24 h / Ambient temperature

With potassium; ammonium chloride; In tetrahydrofuran; benzene;

DOI:10.1021/jo00076a033

upstream raw materials:

2-methoxy-N-methylbenzylamine

2-chloro-ethanol

2-(2-Methoxy-phenyl)-3-methyl-oxazolidine

ortho-anisaldehyde

Downstream raw materials:

3-{2-[(2-methoxy-benzyl)-methyl-amino]-ethoxy}-propionitrile

[2-(3-amino-propoxy)-ethyl]-(2-methoxy-benzyl)-methyl-amine

N-(tert-butoxycarbonylmethyl)-N-(2-hydroxyethyl)-N-(2-methoxybenzyl)-N-methylammonium bromide