(1R,2R,5S,6S)-1,5-Bis-(4-dodecyloxy-phenoxymethyl)-3,7-dimethyl-3,7-diaza-tricyclo[4.2.2.2^2,5]dodeca-9,11-diene-4,8-dione

Base Information

• Chemical Name: (1R,2R,5S,6S)-1,5-Bis-(4-dodecyloxy-phenoxymethyl)-3,7-dimethyl-3,7-diaza-tricyclo[4.2.2.2^2,5]dodeca-9,11-diene-4,8-dione
• CAS No.: 672939-90-1
• Molecular Formula: C₅₀H₇₄N₂O₆
• Molecular Weight: 799.147

Synonyms:(1R,2R,5S,6S)-1,5-Bis-(4-dodecyloxy-phenoxymethyl)-3,7-dimethyl-3,7-diaza-tricyclo[4.2.2.2^2,5]dodeca-9,11-diene-4,8-dione

Chemical Property of (1R,2R,5S,6S)-1,5-Bis-(4-dodecyloxy-phenoxymethyl)-3,7-dimethyl-3,7-diaza-tricyclo[4.2.2.2^2,5]dodeca-9,11-diene-4,8-dione

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Technology Process of (1R,2R,5S,6S)-1,5-Bis-(4-dodecyloxy-phenoxymethyl)-3,7-dimethyl-3,7-diaza-tricyclo[4.2.2.2^2,5]dodeca-9,11-diene-4,8-dione

There total 3 articles about (1R,2R,5S,6S)-1,5-Bis-(4-dodecyloxy-phenoxymethyl)-3,7-dimethyl-3,7-diaza-tricyclo[4.2.2.2^2,5]dodeca-9,11-diene-4,8-dione 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:

3-(chloromethyl)-1-methylpyridin-2(1H)-one (51417-15-3) → (1R,2R,5S,6S)-1,5-Bis-(4-dodecyloxy-phenoxymethyl)-3,7-dimethyl-3,7-diaza-tricyclo[4.2.2.22,5]dodeca-9,11-diene-4,8-dione (672939-90-1)

Guidance literature:

Multi-step reaction with 2 steps

1: 75 percent / K₂CO₃; KI / acetone / Heating

2: 20 h / UV-irradiation

With potassium carbonate; potassium iodide; In acetone; 1: Williamson synthesis;

DOI:10.1021/ol036138e

Reference yield:

4-dodecyloxyphenol (13037-87-1) → (1R,2R,5S,6S)-1,5-Bis-(4-dodecyloxy-phenoxymethyl)-3,7-dimethyl-3,7-diaza-tricyclo[4.2.2.22,5]dodeca-9,11-diene-4,8-dione (672939-90-1)

Guidance literature:

Multi-step reaction with 2 steps

1: 75 percent / K₂CO₃; KI / acetone / Heating

2: 20 h / UV-irradiation

With potassium carbonate; potassium iodide; In acetone; 1: Williamson synthesis;

DOI:10.1021/ol036138e

Reference yield:

3-(4-dodecyloxy-phenoxymethyl)-1-methyl-1H-pyridin-2-one (672939-83-2) → (1R,2R,5S,6S)-1,5-Bis-(4-dodecyloxy-phenoxymethyl)-3,7-dimethyl-3,7-diaza-tricyclo[4.2.2.22,5]dodeca-9,11-diene-4,8-dione (672939-90-1)

Guidance literature:

for 20h; UV-irradiation;

DOI:10.1021/ol036138e

upstream raw materials:

3-(4-dodecyloxy-phenoxymethyl)-1-methyl-1H-pyridin-2-one

3-(chloromethyl)-1-methylpyridin-2(1H)-one

4-dodecyloxyphenol

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