[2-(3-tert-butyldimethylsiloxy-4-methoxystyryl)-5-methyloxazol-4-yl]methanol

Base Information

Chemical Name:[2-(3-tert-butyldimethylsiloxy-4-methoxystyryl)-5-methyloxazol-4-yl]methanol
CAS No.:938071-31-9
Molecular Formula:C₂₀H₂₉NO₄Si
Molecular Weight:375.54
Hs Code.:

Synonyms:[2-(3-tert-butyldimethylsiloxy-4-methoxystyryl)-5-methyloxazol-4-yl]methanol

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Business phase:: The product has achieved commercial mass production^*data from LookChem market partment

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Chemical Property of [2-(3-tert-butyldimethylsiloxy-4-methoxystyryl)-5-methyloxazol-4-yl]methanol

Chemical Property:

Purity/Quality:

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Technology Process of [2-(3-tert-butyldimethylsiloxy-4-methoxystyryl)-5-methyloxazol-4-yl]methanol

There total 5 articles about [2-(3-tert-butyldimethylsiloxy-4-methoxystyryl)-5-methyloxazol-4-yl]methanol 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: 93.0%

: 938071-27-3
methyl 2-(3-tert-butyldimethylsilyloxy-4-methoxystyryl)-5-methyloxazole-4-carboxylate

: 938071-31-9
[2-(3-tert-butyldimethylsiloxy-4-methoxystyryl)-5-methyloxazol-4-yl]methanol

Guidance literature:: With diisobutylaluminium hydride; In dichloromethane;
DOI:10.1039/b618160k

Reference yield:

: 3-hydroxy-4-methoxycinnamamide

: 938071-31-9
[2-(3-tert-butyldimethylsiloxy-4-methoxystyryl)-5-methyloxazol-4-yl]methanol

Guidance literature:: Multi-step reaction with 4 steps

1: 70 percent / imidazole / dimethylformamide

2: 90 percent / dirhodium tetraacetate / CH₂Cl₂ / 4 h / Heating

3: 81 percent / triethylamine; triphenylphosphine; iodine / CH₂Cl₂ / 20 °C

4: 93 percent / DIBAL / CH₂Cl₂

With 1H-imidazole; iodine; diisobutylaluminium hydride; triethylamine; triphenylphosphine; dirhodium tetraacetate; In dichloromethane; N,N-dimethyl-formamide;
DOI:10.1039/b618160k

Reference yield:

: 938071-25-1
(E)-3-(3-tert-butyldimethylsiloxy-4-methoxyphenyl)acrylamide

: 938071-31-9
[2-(3-tert-butyldimethylsiloxy-4-methoxystyryl)-5-methyloxazol-4-yl]methanol

Guidance literature:: Multi-step reaction with 3 steps

1: 90 percent / dirhodium tetraacetate / CH₂Cl₂ / 4 h / Heating

2: 81 percent / triethylamine; triphenylphosphine; iodine / CH₂Cl₂ / 20 °C

3: 93 percent / DIBAL / CH₂Cl₂

With iodine; diisobutylaluminium hydride; triethylamine; triphenylphosphine; dirhodium tetraacetate; In dichloromethane;
DOI:10.1039/b618160k