6-(5-(tert-butyldiphenylsilyloxy)pent-1-ynyl)-2,4-dihydroxy-3-methylbenzaldehyde

Base Information

Chemical Name:6-(5-(tert-butyldiphenylsilyloxy)pent-1-ynyl)-2,4-dihydroxy-3-methylbenzaldehyde
CAS No.:1056013-57-0
Molecular Formula:C₂₉H₃₂O₄Si
Molecular Weight:472.656
Hs Code.:

Synonyms:6-(5-(tert-butyldiphenylsilyloxy)pent-1-ynyl)-2,4-dihydroxy-3-methylbenzaldehyde

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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 6-(5-(tert-butyldiphenylsilyloxy)pent-1-ynyl)-2,4-dihydroxy-3-methylbenzaldehyde

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Technology Process of 6-(5-(tert-butyldiphenylsilyloxy)pent-1-ynyl)-2,4-dihydroxy-3-methylbenzaldehyde

There total 1 articles about 6-(5-(tert-butyldiphenylsilyloxy)pent-1-ynyl)-2,4-dihydroxy-3-methylbenzaldehyde 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: 73.0%

: 91266-03-4
tert-butyl-pent-4-ynyloxy-diphenyl-silane

: 685895-45-8
2-bromo-4,6-dihydroxy-5-methylbenzaldehyde

: 1056013-57-0
6-(5-(tert-butyldiphenylsilyloxy)pent-1-ynyl)-2,4-dihydroxy-3-methylbenzaldehyde

Guidance literature:: With bis-triphenylphosphine-palladium(II) chloride; copper(l) iodide; triethylamine; In N,N-dimethyl-formamide; at 70 ℃; for 16h; Inert atmosphere;
DOI:10.1021/ja8012819

Reference yield: 72.0%

: 1056013-57-0
6-(5-(tert-butyldiphenylsilyloxy)pent-1-ynyl)-2,4-dihydroxy-3-methylbenzaldehyde

: 1056013-58-1
3-(3-tert-butyldiphenylsilyloxypropyl)-7-hydroxy-7-methyl-6H-isochromene-6,8-dione

Guidance literature:: 6-(5-(tert-butyldiphenylsilyloxy)pent-1-ynyl)-2,4-dihydroxy-3-methylbenzaldehyde; With gold(lll) acetate; trifluoroacetic acid; In 1,2-dichloro-ethane; at 23 ℃; for 0.0666667h;

With tetra-(n-butyl)ammonium iodide; 1-hydroxy-3H-benz[d][1,2]iodoxole-1,3-dione; In 1,2-dichloro-ethane; at 23 ℃; for 4h;
DOI:10.1021/ja8012819