2-(4-(4-methoxybenzyloxy)butyl)-4,6-dimethyl-3,5-di((Z)-dec-1-enyl)pyridine

Base Information

Chemical Name:2-(4-(4-methoxybenzyloxy)butyl)-4,6-dimethyl-3,5-di((Z)-dec-1-enyl)pyridine
CAS No.:1334291-30-3
Molecular Formula:C₃₉H₆₁NO₂
Molecular Weight:575.919
Hs Code.:

Synonyms:2-(4-(4-methoxybenzyloxy)butyl)-4,6-dimethyl-3,5-di((Z)-dec-1-enyl)pyridine

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Chemical Property of 2-(4-(4-methoxybenzyloxy)butyl)-4,6-dimethyl-3,5-di((Z)-dec-1-enyl)pyridine

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Technology Process of 2-(4-(4-methoxybenzyloxy)butyl)-4,6-dimethyl-3,5-di((Z)-dec-1-enyl)pyridine

There total 7 articles about 2-(4-(4-methoxybenzyloxy)butyl)-4,6-dimethyl-3,5-di((Z)-dec-1-enyl)pyridine 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:

: 1334291-29-0
C₂₁H₂₅NO₄

: 60902-45-6
nonyltriphenylphosphonium bromide

: 2-(4-(4-methoxybenzyloxy)butyl)-4,6-dimethyl-3,5-di(dec-1-enyl)pyridine

: 1334291-30-3
2-(4-(4-methoxybenzyloxy)butyl)-4,6-dimethyl-3,5-di((Z)-dec-1-enyl)pyridine

: 1334291-38-1
2-(4-(4-methoxybenzyloxy)butyl)-4,6-dimethyl-3,5-di((E)-dec-1-enyl)pyridine

Guidance literature:: With lithium hexamethyldisilazane; In tetrahydrofuran; toluene; at -70 - 20 ℃; for 1h; Inert atmosphere;
DOI:10.1016/j.bmcl.2011.07.058

Reference yield:

: 1334291-27-8
2-(4-(4-methoxybenzyloxy)but-1-ynyl)-4,6-dimethylpyridine-3,5-dicarbonitrile

: 1334291-30-3
2-(4-(4-methoxybenzyloxy)butyl)-4,6-dimethyl-3,5-di((Z)-dec-1-enyl)pyridine

: 1334291-38-1
2-(4-(4-methoxybenzyloxy)butyl)-4,6-dimethyl-3,5-di((E)-dec-1-enyl)pyridine

Guidance literature:: Multi-step reaction with 3 steps

1: 5%-palladium/activated carbon; hydrogen / methanol / 6 h / 20 °C / 2999.54 Torr

2: diisobutylaluminium hydride / toluene / 0.83 h / -15 - 0 °C / Inert atmosphere

3: lithium hexamethyldisilazane / tetrahydrofuran; toluene / 1 h / -70 - 20 °C / Inert atmosphere

With 5%-palladium/activated carbon; hydrogen; diisobutylaluminium hydride; lithium hexamethyldisilazane; In tetrahydrofuran; methanol; toluene; 3: Wittig reaction;
DOI:10.1016/j.bmcl.2011.07.058

Reference yield:

: 1334291-28-9
2-(4-(4-methoxybenzyloxy)butyl)-4,6-dimethylpyridine-3,5-dicarbonitrile

: 1334291-30-3
2-(4-(4-methoxybenzyloxy)butyl)-4,6-dimethyl-3,5-di((Z)-dec-1-enyl)pyridine

: 1334291-38-1
2-(4-(4-methoxybenzyloxy)butyl)-4,6-dimethyl-3,5-di((E)-dec-1-enyl)pyridine

Guidance literature:: Multi-step reaction with 2 steps

1: diisobutylaluminium hydride / toluene / 0.83 h / -15 - 0 °C / Inert atmosphere

2: lithium hexamethyldisilazane / tetrahydrofuran; toluene / 1 h / -70 - 20 °C / Inert atmosphere

With diisobutylaluminium hydride; lithium hexamethyldisilazane; In tetrahydrofuran; toluene; 2: Wittig reaction;
DOI:10.1016/j.bmcl.2011.07.058