3-[(R,2E,4E)-6-(hydroxymethyl)-4-methylocta-2,4-dienoyl]-4-methoxy-5-[4-(4-methoxybenzyloxy)phenyl]pyridin-2(1H)-one

Base Information

Chemical Name:3-[(R,2E,4E)-6-(hydroxymethyl)-4-methylocta-2,4-dienoyl]-4-methoxy-5-[4-(4-methoxybenzyloxy)phenyl]pyridin-2(1H)-one
CAS No.:1629189-51-0
Molecular Formula:C₃₀H₃₃NO₆
Molecular Weight:503.595
Hs Code.:

Synonyms:3-[(R,2E,4E)-6-(hydroxymethyl)-4-methylocta-2,4-dienoyl]-4-methoxy-5-[4-(4-methoxybenzyloxy)phenyl]pyridin-2(1H)-one

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Chemical Property of 3-[(R,2E,4E)-6-(hydroxymethyl)-4-methylocta-2,4-dienoyl]-4-methoxy-5-[4-(4-methoxybenzyloxy)phenyl]pyridin-2(1H)-one

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Technology Process of 3-[(R,2E,4E)-6-(hydroxymethyl)-4-methylocta-2,4-dienoyl]-4-methoxy-5-[4-(4-methoxybenzyloxy)phenyl]pyridin-2(1H)-one

There total 7 articles about 3-[(R,2E,4E)-6-(hydroxymethyl)-4-methylocta-2,4-dienoyl]-4-methoxy-5-[4-(4-methoxybenzyloxy)phenyl]pyridin-2(1H)-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%

: 1309567-75-6
dimethyl (2-(4-methoxy-5-(4-((4-methoxybenzyl)oxy)phenyl)-2-oxo-1,2-dihydropyridin-3-yl)-2-oxoethyl)phosphonate

: 1629189-47-4
(R,E)-4-(hydroxymethyl)-2-methylhex-2-enal

: 1629189-51-0
3-[(R,2E,4E)-6-(hydroxymethyl)-4-methylocta-2,4-dienoyl]-4-methoxy-5-[4-(4-methoxybenzyloxy)phenyl]pyridin-2(1H)-one

Guidance literature:: With lithium hydroxide monohydrate; In tetrahydrofuran; water; at 20 ℃; for 144h; Darkness;
DOI:10.1055/s-0033-1340868

Reference yield:

: 1321530-55-5
(S)-methyl 2-(((tert-butyldiphenylsilyl)oxy)methyl)butanoate

: 1629189-51-0
3-[(R,2E,4E)-6-(hydroxymethyl)-4-methylocta-2,4-dienoyl]-4-methoxy-5-[4-(4-methoxybenzyloxy)phenyl]pyridin-2(1H)-one

Guidance literature:: Multi-step reaction with 6 steps

1: diisobutylaluminium hydride / dichloromethane / 1 h / -78 °C

2: dichloromethane / 48 h / Reflux

3: diisobutylaluminium hydride / tetrahydrofuran; hexane / 1.83 h / -78 - 20 °C

4: 4-methylmorpholine N-oxide; tetrapropylammonium perruthennate / dichloromethane / 1 h / 20 °C / Molecular sieve

5: tetrabutyl ammonium fluoride / tetrahydrofuran / 2 h / 20 °C

6: lithium hydroxide monohydrate / water; tetrahydrofuran / 144 h / 20 °C / Darkness

With tetrapropylammonium perruthennate; lithium hydroxide monohydrate; tetrabutyl ammonium fluoride; diisobutylaluminium hydride; 4-methylmorpholine N-oxide; In tetrahydrofuran; hexane; dichloromethane; water;
DOI:10.1055/s-0033-1340868

Reference yield:

: 1629189-45-2
ethyl (R,E)-4-[(tert-butyldiphenylsiloxy)methyl]-2-methylhex-2-enoate

: 1629189-51-0
3-[(R,2E,4E)-6-(hydroxymethyl)-4-methylocta-2,4-dienoyl]-4-methoxy-5-[4-(4-methoxybenzyloxy)phenyl]pyridin-2(1H)-one

Guidance literature:: Multi-step reaction with 4 steps

1: diisobutylaluminium hydride / tetrahydrofuran; hexane / 1.83 h / -78 - 20 °C

2: 4-methylmorpholine N-oxide; tetrapropylammonium perruthennate / dichloromethane / 1 h / 20 °C / Molecular sieve

3: tetrabutyl ammonium fluoride / tetrahydrofuran / 2 h / 20 °C

4: lithium hydroxide monohydrate / water; tetrahydrofuran / 144 h / 20 °C / Darkness

With tetrapropylammonium perruthennate; lithium hydroxide monohydrate; tetrabutyl ammonium fluoride; diisobutylaluminium hydride; 4-methylmorpholine N-oxide; In tetrahydrofuran; hexane; dichloromethane; water;
DOI:10.1055/s-0033-1340868