methyl N-methyl-<4-<2-<(2-hydroxy-3-phenoxypropyl)amino>ethoxy>phenoxy>acetate

Base Information

Chemical Name:methyl N-methyl-<4-<2-<(2-hydroxy-3-phenoxypropyl)amino>ethoxy>phenoxy>acetate
CAS No.:140662-56-2
Molecular Formula:C₂₁H₂₇NO₆
Molecular Weight:389.448
Hs Code.:

Synonyms:methyl N-methyl-<4-<2-<(2-hydroxy-3-phenoxypropyl)amino>ethoxy>phenoxy>acetate

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Chemical Property of methyl N-methyl-<4-<2-<(2-hydroxy-3-phenoxypropyl)amino>ethoxy>phenoxy>acetate

Chemical Property:

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Technology Process of methyl N-methyl-<4-<2-<(2-hydroxy-3-phenoxypropyl)amino>ethoxy>phenoxy>acetate

There total 5 articles about methyl N-methyl-<4-<2-<(2-hydroxy-3-phenoxypropyl)amino>ethoxy>phenoxy>acetate 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:

: 122-60-1,71031-02-2
Phenyl glycidyl ether

: 140662-56-2
methyl N-methyl-<4-<2-<(2-hydroxy-3-phenoxypropyl)amino>ethoxy>phenoxy>acetate

Guidance literature:: Multi-step reaction with 4 steps

1: propan-2-ol / 72 h / Heating

2: K₂CO₃, KI / acetone / 24 h / Heating

3: H₂, AcOH / 10percent Pd/C / methanol / 48 h / 60 °C / 15001.2 Torr

4: formic acid / H₂O / 3 h / 100 °C

With formic acid; hydrogen; potassium carbonate; acetic acid; potassium iodide; palladium on activated charcoal; In methanol; water; isopropyl alcohol; acetone;
DOI:10.1021/jm00088a010

Reference yield:

: 107332-60-5
N-benzyl-N-<2-(4-hydroxyphenoxy)ethyl>-2-hydroxy-3-phenoxypropylamine

: 140662-56-2
methyl N-methyl-<4-<2-<(2-hydroxy-3-phenoxypropyl)amino>ethoxy>phenoxy>acetate

Guidance literature:: Multi-step reaction with 3 steps

1: K₂CO₃, KI / acetone / 24 h / Heating

2: H₂, AcOH / 10percent Pd/C / methanol / 48 h / 60 °C / 15001.2 Torr

3: formic acid / H₂O / 3 h / 100 °C

With formic acid; hydrogen; potassium carbonate; acetic acid; potassium iodide; palladium on activated charcoal; In methanol; water; acetone;
DOI:10.1021/jm00088a010

Reference yield:

: 107332-63-8
N-benzyl-2-(4-hydroxyphenoxy)ethylamine hydrochloride

: 140662-56-2
methyl N-methyl-<4-<2-<(2-hydroxy-3-phenoxypropyl)amino>ethoxy>phenoxy>acetate

Guidance literature:: Multi-step reaction with 4 steps

1: propan-2-ol / 72 h / Heating

2: K₂CO₃, KI / acetone / 24 h / Heating

3: H₂, AcOH / 10percent Pd/C / methanol / 48 h / 60 °C / 15001.2 Torr

4: formic acid / H₂O / 3 h / 100 °C

With formic acid; hydrogen; potassium carbonate; acetic acid; potassium iodide; palladium on activated charcoal; In methanol; water; isopropyl alcohol; acetone;
DOI:10.1021/jm00088a010