3-(4-cyclopropylphenoxy)-1-(3-methoxy-4-(2-((tetrahydro-2H-pyran-2-yl)oxy)ethoxy)phenyl)-1H-pyrrol-2(5H)-one

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Chemical Name:3-(4-cyclopropylphenoxy)-1-(3-methoxy-4-(2-((tetrahydro-2H-pyran-2-yl)oxy)ethoxy)phenyl)-1H-pyrrol-2(5H)-one
CAS No.:1574541-83-5
Molecular Formula:C₂₇H₃₁NO₆
Molecular Weight:465.546
Hs Code.:

Synonyms:3-(4-cyclopropylphenoxy)-1-(3-methoxy-4-(2-((tetrahydro-2H-pyran-2-yl)oxy)ethoxy)phenyl)-1H-pyrrol-2(5H)-one

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Chemical Property of 3-(4-cyclopropylphenoxy)-1-(3-methoxy-4-(2-((tetrahydro-2H-pyran-2-yl)oxy)ethoxy)phenyl)-1H-pyrrol-2(5H)-one

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Purity/Quality:: 98% ^*data from raw suppliers

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Technology Process of 3-(4-cyclopropylphenoxy)-1-(3-methoxy-4-(2-((tetrahydro-2H-pyran-2-yl)oxy)ethoxy)phenyl)-1H-pyrrol-2(5H)-one

There total 9 articles about 3-(4-cyclopropylphenoxy)-1-(3-methoxy-4-(2-((tetrahydro-2H-pyran-2-yl)oxy)ethoxy)phenyl)-1H-pyrrol-2(5H)-one 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: 77.0%

: 1574541-82-4
N-allyl-2-(4-cyclopropylphenoxy)-N-(3-methoxy-4-(2-((tetrahydro-2H-pyran-2-yl)oxy)ethoxy)phenyl)but-2-enamide

: 1574541-83-5
3-(4-cyclopropylphenoxy)-1-(3-methoxy-4-(2-((tetrahydro-2H-pyran-2-yl)oxy)ethoxy)phenyl)-1H-pyrrol-2(5H)-one

Guidance literature:: With tricyclohexylphosphine[1,3-bis(2,4,6-trimethylphenyl)-4,5-dihydroimidazol-2-ylidine][benzylidene]ruthenium(II) dichloride; In toluene; at 80 ℃; for 12h; Inert atmosphere;

Reference yield:

: 1574541-77-7
methyl 2-(4-cyclopropylphenoxy)but-2-enoate

: 1574541-83-5
3-(4-cyclopropylphenoxy)-1-(3-methoxy-4-(2-((tetrahydro-2H-pyran-2-yl)oxy)ethoxy)phenyl)-1H-pyrrol-2(5H)-one

Guidance literature:: Multi-step reaction with 4 steps

1.1: lithium hydroxide monohydrate; water / tetrahydrofuran / 0 - 20 °C

2.1: triethylamine; benzotriazol-1-ol; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride / acetonitrile / 0 - 20 °C / Inert atmosphere

3.1: sodium hydride / N,N-dimethyl-formamide / 1 h / 0 °C

3.2: 6 h

4.1: tricyclohexylphosphine[1,3-bis(2,4,6-trimethylphenyl)-4,5-dihydroimidazol-2-ylidine][benzylidene]ruthenium(II) dichloride / toluene / 12 h / 80 °C / Inert atmosphere

With tricyclohexylphosphine[1,3-bis(2,4,6-trimethylphenyl)-4,5-dihydroimidazol-2-ylidine][benzylidene]ruthenium(II) dichloride; lithium hydroxide monohydrate; water; sodium hydride; benzotriazol-1-ol; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride; triethylamine; In tetrahydrofuran; N,N-dimethyl-formamide; toluene; acetonitrile;

Reference yield:

: 1574541-78-8
2-(4-cyclopropylphenoxy)but-2-enoic acid

: 1574541-83-5
3-(4-cyclopropylphenoxy)-1-(3-methoxy-4-(2-((tetrahydro-2H-pyran-2-yl)oxy)ethoxy)phenyl)-1H-pyrrol-2(5H)-one

Guidance literature:: Multi-step reaction with 3 steps

1.1: triethylamine; benzotriazol-1-ol; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride / acetonitrile / 0 - 20 °C / Inert atmosphere

2.1: sodium hydride / N,N-dimethyl-formamide / 1 h / 0 °C

2.2: 6 h

3.1: tricyclohexylphosphine[1,3-bis(2,4,6-trimethylphenyl)-4,5-dihydroimidazol-2-ylidine][benzylidene]ruthenium(II) dichloride / toluene / 12 h / 80 °C / Inert atmosphere

With tricyclohexylphosphine[1,3-bis(2,4,6-trimethylphenyl)-4,5-dihydroimidazol-2-ylidine][benzylidene]ruthenium(II) dichloride; sodium hydride; benzotriazol-1-ol; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride; triethylamine; In N,N-dimethyl-formamide; toluene; acetonitrile;