2-<(2-Hydroxyethyl)benzylamino>-1-<(2-methyl-1,3-dioxolan-2-yl)methyl>ethyltriphenylphosphonium iodide

Base Information

Chemical Name:2-<(2-Hydroxyethyl)benzylamino>-1-<(2-methyl-1,3-dioxolan-2-yl)methyl>ethyltriphenylphosphonium iodide
CAS No.:123420-22-4
Molecular Formula:C₃₄H₃₉NO₃P*I
Molecular Weight:667.567
Hs Code.:

Synonyms:2-<(2-Hydroxyethyl)benzylamino>-1-<(2-methyl-1,3-dioxolan-2-yl)methyl>ethyltriphenylphosphonium iodide

Suppliers and Price of 2-<(2-Hydroxyethyl)benzylamino>-1-<(2-methyl-1,3-dioxolan-2-yl)methyl>ethyltriphenylphosphonium iodide

Supply Marketing:

Business phase:: The product has achieved commercial mass production^*data from LookChem market partment

Manufacturers and distributors:

Manufacture/Brand
Chemicals and raw materials
Packaging
price

Total 0 raw suppliers

Chemical Property of 2-<(2-Hydroxyethyl)benzylamino>-1-<(2-methyl-1,3-dioxolan-2-yl)methyl>ethyltriphenylphosphonium iodide

Chemical Property:

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:

Useful:

Technology Process of 2-<(2-Hydroxyethyl)benzylamino>-1-<(2-methyl-1,3-dioxolan-2-yl)methyl>ethyltriphenylphosphonium iodide

There total 1 articles about 2-<(2-Hydroxyethyl)benzylamino>-1-<(2-methyl-1,3-dioxolan-2-yl)methyl>ethyltriphenylphosphonium iodide 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: 85.0%

: 82777-75-1
1-<(2-Methyl-1,3-dioxolan-2-yl)methyl>ethenyltriphenylphosphonium iodide

: 104-63-2
N-Benzylethanolamine

: 123420-22-4
2-<(2-Hydroxyethyl)benzylamino>-1-<(2-methyl-1,3-dioxolan-2-yl)methyl>ethyltriphenylphosphonium iodide

Guidance literature:: In acetonitrile; for 96h; Ambient temperature;
DOI:10.1055/s-1989-27232

Reference yield: 86.0%

: 123420-22-4
2-<(2-Hydroxyethyl)benzylamino>-1-<(2-methyl-1,3-dioxolan-2-yl)methyl>ethyltriphenylphosphonium iodide

: 123420-25-7
2-Acetonyl-4-benzylmorpholine

Guidance literature:: With sulfuric acid; In acetone; for 48h; Heating;
DOI:10.1055/s-1989-27232

Reference yield:

: 123420-22-4
2-<(2-Hydroxyethyl)benzylamino>-1-<(2-methyl-1,3-dioxolan-2-yl)methyl>ethyltriphenylphosphonium iodide

: 123420-26-8
2-Acetonylmorpholine

Guidance literature:: Multi-step reaction with 2 steps

1: 86 percent / 4 N aq. H₂SO₄ / acetone / 48 h / Heating

2: 70 percent / H₂, conc. aq. HCl / 10percent Pd/C / methanol / 10 h / Ambient temperature

With hydrogenchloride; sulfuric acid; hydrogen; palladium on activated charcoal; In methanol; acetone;
DOI:10.1055/s-1989-27232