1-<2-hydroxy-4-<<2-(2-hydroxyethyl)phenyl>methoxy>-3-propylphenyl>ethanone

Base Information

Chemical Name:1-<2-hydroxy-4-<<2-(2-hydroxyethyl)phenyl>methoxy>-3-propylphenyl>ethanone
CAS No.:122443-68-9
Molecular Formula:C₂₀H₂₄O₄
Molecular Weight:328.408
Hs Code.:

Synonyms:1-<2-hydroxy-4-<<2-(2-hydroxyethyl)phenyl>methoxy>-3-propylphenyl>ethanone

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Chemical Property of 1-<2-hydroxy-4-<<2-(2-hydroxyethyl)phenyl>methoxy>-3-propylphenyl>ethanone

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Technology Process of 1-<2-hydroxy-4-<<2-(2-hydroxyethyl)phenyl>methoxy>-3-propylphenyl>ethanone

There total 4 articles about 1-<2-hydroxy-4-<<2-(2-hydroxyethyl)phenyl>methoxy>-3-propylphenyl>ethanone 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: 79.5%

: 122443-67-8
1-(2-Hydroxy-3-propyl-4-{2-[2-(tetrahydro-pyran-2-yloxy)-ethyl]-benzyloxy}-phenyl)-ethanone

: 122443-68-9
1-<2-hydroxy-4-<<2-(2-hydroxyethyl)phenyl>methoxy>-3-propylphenyl>ethanone

Guidance literature:: With hydrogenchloride; In tetrahydrofuran; for 20h; Ambient temperature;
DOI:10.1021/jm00128a028

Reference yield:

: 493-05-0
isochromane

: 122443-68-9
1-<2-hydroxy-4-<<2-(2-hydroxyethyl)phenyl>methoxy>-3-propylphenyl>ethanone

Guidance literature:: Multi-step reaction with 4 steps

1: 63.5 percent / HBr / 17 h / Ambient temperature

2: 78.6 percent / p-toluenesulfonic acid monohydrate / diethyl ether / 4 h / Ambient temperature

3: 90 percent / K₂CO₃ / 18-crown-6 / acetonitrile / 17 h / Heating

4: 79.5 percent / 2 N HCl / tetrahydrofuran / 20 h / Ambient temperature

With hydrogenchloride; hydrogen bromide; potassium carbonate; toluene-4-sulfonic acid; 18-crown-6 ether; In tetrahydrofuran; diethyl ether; acetonitrile;
DOI:10.1021/jm00128a028

Reference yield:

: 122444-35-3
2-(2-bromomethyl)-phenethyl alcohol

: 122443-68-9
1-<2-hydroxy-4-<<2-(2-hydroxyethyl)phenyl>methoxy>-3-propylphenyl>ethanone

Guidance literature:: Multi-step reaction with 3 steps

1: 78.6 percent / p-toluenesulfonic acid monohydrate / diethyl ether / 4 h / Ambient temperature

2: 90 percent / K₂CO₃ / 18-crown-6 / acetonitrile / 17 h / Heating

3: 79.5 percent / 2 N HCl / tetrahydrofuran / 20 h / Ambient temperature

With hydrogenchloride; potassium carbonate; toluene-4-sulfonic acid; 18-crown-6 ether; In tetrahydrofuran; diethyl ether; acetonitrile;
DOI:10.1021/jm00128a028