2-(4-hydroxy-2,6-dimethylphenyl)-3-methoxy-5-(tetrahydropyran-4-ylmethyl)cyclopent-2-enone

Base Information

Chemical Name:2-(4-hydroxy-2,6-dimethylphenyl)-3-methoxy-5-(tetrahydropyran-4-ylmethyl)cyclopent-2-enone
CAS No.:1237529-59-7
Molecular Formula:C₂₀H₂₆O₄
Molecular Weight:330.424
Hs Code.:

Synonyms:2-(4-hydroxy-2,6-dimethylphenyl)-3-methoxy-5-(tetrahydropyran-4-ylmethyl)cyclopent-2-enone

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Chemical Property of 2-(4-hydroxy-2,6-dimethylphenyl)-3-methoxy-5-(tetrahydropyran-4-ylmethyl)cyclopent-2-enone

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Technology Process of 2-(4-hydroxy-2,6-dimethylphenyl)-3-methoxy-5-(tetrahydropyran-4-ylmethyl)cyclopent-2-enone

There total 5 articles about 2-(4-hydroxy-2,6-dimethylphenyl)-3-methoxy-5-(tetrahydropyran-4-ylmethyl)cyclopent-2-enone 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:

: 50675-18-8
3,4,5,6-tetrahydro-2H-pyran-4-carbaldehyde

: 1237529-59-7
2-(4-hydroxy-2,6-dimethylphenyl)-3-methoxy-5-(tetrahydropyran-4-ylmethyl)cyclopent-2-enone

Guidance literature:: Multi-step reaction with 2 steps

1.1: lithium diisopropyl amide / tetrahydrofuran / 0.52 h / -78 °C / Inert atmosphere

1.2: -78 - 20 °C

1.3: 1 h / 20 °C

2.1: hydrogen / 5%-palladium/activated carbon / ethanol / 4 h / 3000.3 Torr

With hydrogen; lithium diisopropyl amide; 5%-palladium/activated carbon; In tetrahydrofuran; ethanol;

Reference yield:

: 1237529-58-6
2-(4-benzyloxy-2,6-dimethylphenyl)-3-methoxy-5-[1-(tetrahydropyran-4-yl)-methylidene]cyclopent-2-enone

: 1237529-59-7
2-(4-hydroxy-2,6-dimethylphenyl)-3-methoxy-5-(tetrahydropyran-4-ylmethyl)cyclopent-2-enone

Guidance literature:: With hydrogen; 5%-palladium/activated carbon; In ethanol; for 4h; under 3000.3 Torr;

Reference yield:

: 865139-18-0
(4-(benzyloxy)-2,6-dimethylphenyl)boronic acid

: 1237529-59-7
2-(4-hydroxy-2,6-dimethylphenyl)-3-methoxy-5-(tetrahydropyran-4-ylmethyl)cyclopent-2-enone

Guidance literature:: Multi-step reaction with 3 steps

1.1: potassium phosphate / dicyclohexyl-(2',6'-dimethoxybiphenyl-2-yl)-phosphane; palladium diacetate / toluene / 4 h / 90 °C / Inert atmosphere

2.1: lithium diisopropyl amide / tetrahydrofuran / 0.52 h / -78 °C / Inert atmosphere

2.2: -78 - 20 °C

2.3: 1 h / 20 °C

3.1: hydrogen / 5%-palladium/activated carbon / ethanol / 4 h / 3000.3 Torr

With potassium phosphate; hydrogen; lithium diisopropyl amide; dicyclohexyl-(2',6'-dimethoxybiphenyl-2-yl)-phosphane; 5%-palladium/activated carbon; palladium diacetate; In tetrahydrofuran; ethanol; toluene;