(E)-methyl 2-(2-(3-((tert-butyldimethylsilyl)oxy)-9-((4-methoxybenzyl)oxy)-2-methyl-7-oxonon-5-en-2-yl)thiazol-4-yl)acetate

Base Information

Chemical Name:(E)-methyl 2-(2-(3-((tert-butyldimethylsilyl)oxy)-9-((4-methoxybenzyl)oxy)-2-methyl-7-oxonon-5-en-2-yl)thiazol-4-yl)acetate
CAS No.:1352739-37-7
Molecular Formula:C₃₀H₄₅NO₆SSi
Molecular Weight:575.842
Hs Code.:

Synonyms:(E)-methyl 2-(2-(3-((tert-butyldimethylsilyl)oxy)-9-((4-methoxybenzyl)oxy)-2-methyl-7-oxonon-5-en-2-yl)thiazol-4-yl)acetate

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Chemical Property of (E)-methyl 2-(2-(3-((tert-butyldimethylsilyl)oxy)-9-((4-methoxybenzyl)oxy)-2-methyl-7-oxonon-5-en-2-yl)thiazol-4-yl)acetate

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Technology Process of (E)-methyl 2-(2-(3-((tert-butyldimethylsilyl)oxy)-9-((4-methoxybenzyl)oxy)-2-methyl-7-oxonon-5-en-2-yl)thiazol-4-yl)acetate

There total 16 articles about (E)-methyl 2-(2-(3-((tert-butyldimethylsilyl)oxy)-9-((4-methoxybenzyl)oxy)-2-methyl-7-oxonon-5-en-2-yl)thiazol-4-yl)acetate 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: 83.0%

: 1352739-31-1
5-[(4-methoxybenzyl)oxy]pent-1-en-3-one

: 1352739-36-6
methyl 2-(2-{3-[(tert-butyldimethylsilyl)oxy]-2-methylhex-5-en-2-yl}thiazol-4-yl)acetate

: 1352739-37-7
(E)-methyl 2-(2-(3-((tert-butyldimethylsilyl)oxy)-9-((4-methoxybenzyl)oxy)-2-methyl-7-oxonon-5-en-2-yl)thiazol-4-yl)acetate

Guidance literature:: With tricyclohexylphosphine[1,3-bis(2,4,6-trimethylphenyl)-4,5-dihydroimidazol-2-ylidine][benzylidene]ruthenium(II) dichloride; In dichloromethane; at 50 ℃; for 0.25h; Inert atmosphere; Microwave irradiation;
DOI:10.1002/ejoc.201100669

Reference yield:

: 1352739-32-2
methyl 2-[2-(3-hydroxy-2-methylhex-5-en-2-yl)thiazol-4-yl]acetate

: 1352739-37-7
(E)-methyl 2-(2-(3-((tert-butyldimethylsilyl)oxy)-9-((4-methoxybenzyl)oxy)-2-methyl-7-oxonon-5-en-2-yl)thiazol-4-yl)acetate

Guidance literature:: Multi-step reaction with 2 steps

1: 2,6-dimethylpyridine / dichloromethane / 1 h / -78 °C / Inert atmosphere

2: tricyclohexylphosphine[1,3-bis(2,4,6-trimethylphenyl)-4,5-dihydroimidazol-2-ylidine][benzylidene]ruthenium(II) dichloride / dichloromethane / 0.25 h / 50 °C / Inert atmosphere; Microwave irradiation

With tricyclohexylphosphine[1,3-bis(2,4,6-trimethylphenyl)-4,5-dihydroimidazol-2-ylidine][benzylidene]ruthenium(II) dichloride; 2,6-dimethylpyridine; In dichloromethane;
DOI:10.1002/ejoc.201100669

Reference yield:

: 1226985-26-7
(+/-)-5-(4-methoxybenzyloxy)pent-1-en-3-ol

: 1352739-37-7
(E)-methyl 2-(2-(3-((tert-butyldimethylsilyl)oxy)-9-((4-methoxybenzyl)oxy)-2-methyl-7-oxonon-5-en-2-yl)thiazol-4-yl)acetate

Guidance literature:: Multi-step reaction with 2 steps

1: 2-iodoxybenzoic acid / tetrahydrofuran; dimethyl sulfoxide / 6 h / Inert atmosphere

2: tricyclohexylphosphine[1,3-bis(2,4,6-trimethylphenyl)-4,5-dihydroimidazol-2-ylidine][benzylidene]ruthenium(II) dichloride / dichloromethane / 0.25 h / 50 °C / Inert atmosphere; Microwave irradiation

With tricyclohexylphosphine[1,3-bis(2,4,6-trimethylphenyl)-4,5-dihydroimidazol-2-ylidine][benzylidene]ruthenium(II) dichloride; 2-iodoxybenzoic acid; In tetrahydrofuran; dichloromethane; dimethyl sulfoxide;
DOI:10.1002/ejoc.201100669