2-(2,6-dimethyl-4-prop-1-ynylphenyl)-3-(methoxycarbonyloxy)-5-(pyridin-2-yl)cyclohex-2-en-1-one

Base Information

Chemical Name:2-(2,6-dimethyl-4-prop-1-ynylphenyl)-3-(methoxycarbonyloxy)-5-(pyridin-2-yl)cyclohex-2-en-1-one
CAS No.:1615201-93-8
Molecular Formula:C₂₄H₂₃NO₄
Molecular Weight:389.451
Hs Code.:

Synonyms:2-(2,6-dimethyl-4-prop-1-ynylphenyl)-3-(methoxycarbonyloxy)-5-(pyridin-2-yl)cyclohex-2-en-1-one

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Chemical Property of 2-(2,6-dimethyl-4-prop-1-ynylphenyl)-3-(methoxycarbonyloxy)-5-(pyridin-2-yl)cyclohex-2-en-1-one

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Technology Process of 2-(2,6-dimethyl-4-prop-1-ynylphenyl)-3-(methoxycarbonyloxy)-5-(pyridin-2-yl)cyclohex-2-en-1-one

There total 10 articles about 2-(2,6-dimethyl-4-prop-1-ynylphenyl)-3-(methoxycarbonyloxy)-5-(pyridin-2-yl)cyclohex-2-en-1-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: 96.0%

: 1615201-92-7
2-(2,6-dimethyl-4-prop-1-ynylphenyl)-5-(pyridin-2-yl)cyclohexane-1,3-dione hydrochloride

: 79-22-1
methyl chloroformate

: 1615201-93-8
2-(2,6-dimethyl-4-prop-1-ynylphenyl)-3-(methoxycarbonyloxy)-5-(pyridin-2-yl)cyclohex-2-en-1-one

Guidance literature:: With triethylamine; In dichloromethane; at 20 ℃; for 18h;

Reference yield:

: 1615211-89-6
1-(4-bromo-2,6-dimethylphenyl)propan

: 1615201-93-8
2-(2,6-dimethyl-4-prop-1-ynylphenyl)-3-(methoxycarbonyloxy)-5-(pyridin-2-yl)cyclohex-2-en-1-one

Guidance literature:: Multi-step reaction with 7 steps

1.1: sodium hydroxide / water; ethanol / 0.08 h / 20 °C

2.1: sodium methylate / methanol / 0.17 h / 20 °C

2.2: 24 h / Reflux

3.1: sulfuric acid / water / 4 h / Reflux

4.1: potassium carbonate / acetone / 18 h / 20 °C

5.1: copper(l) iodide; cesium fluoride; (1,1'-bis(diphenylphosphino)ferrocene)palladium(II) dichloride / N,N-dimethyl-formamide / 1 h / 120 °C / Inert atmosphere; Microwave irradiation

6.1: hydrogenchloride / water; acetone / 70 - 90 °C / Microwave irradiation

7.1: triethylamine / dichloromethane / 18 h / 20 °C

With hydrogenchloride; (1,1'-bis(diphenylphosphino)ferrocene)palladium(II) dichloride; copper(l) iodide; sulfuric acid; sodium methylate; potassium carbonate; triethylamine; cesium fluoride; sodium hydroxide; In methanol; ethanol; dichloromethane; water; N,N-dimethyl-formamide; acetone;

Reference yield:

: 1615211-90-9
1-(4-bromo-2,6-dimethylphenyl)-4-(pyridin-2-yl)but-3-en-2-one

: 1615201-93-8
2-(2,6-dimethyl-4-prop-1-ynylphenyl)-3-(methoxycarbonyloxy)-5-(pyridin-2-yl)cyclohex-2-en-1-one

Guidance literature:: Multi-step reaction with 6 steps

1.1: sodium methylate / methanol / 0.17 h / 20 °C

1.2: 24 h / Reflux

2.1: sulfuric acid / water / 4 h / Reflux

3.1: potassium carbonate / acetone / 18 h / 20 °C

4.1: copper(l) iodide; cesium fluoride; (1,1'-bis(diphenylphosphino)ferrocene)palladium(II) dichloride / N,N-dimethyl-formamide / 1 h / 120 °C / Inert atmosphere; Microwave irradiation

5.1: hydrogenchloride / water; acetone / 70 - 90 °C / Microwave irradiation

6.1: triethylamine / dichloromethane / 18 h / 20 °C

With hydrogenchloride; (1,1'-bis(diphenylphosphino)ferrocene)palladium(II) dichloride; copper(l) iodide; sulfuric acid; sodium methylate; potassium carbonate; triethylamine; cesium fluoride; In methanol; dichloromethane; water; N,N-dimethyl-formamide; acetone;