3-<3,4-di(tert-butyldimethylsilyloxy)phenyl>-5-(2,4-dihydroxyphenyl)isoxazole

Base Information

Chemical Name:3-<3,4-di(tert-butyldimethylsilyloxy)phenyl>-5-(2,4-dihydroxyphenyl)isoxazole
CAS No.:169693-89-4
Molecular Formula:C₂₇H₃₉NO₅Si₂
Molecular Weight:513.781
Hs Code.:

Synonyms:3-<3,4-di(tert-butyldimethylsilyloxy)phenyl>-5-(2,4-dihydroxyphenyl)isoxazole

Suppliers and Price of 3-<3,4-di(tert-butyldimethylsilyloxy)phenyl>-5-(2,4-dihydroxyphenyl)isoxazole

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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 3-<3,4-di(tert-butyldimethylsilyloxy)phenyl>-5-(2,4-dihydroxyphenyl)isoxazole

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Technology Process of 3-<3,4-di(tert-butyldimethylsilyloxy)phenyl>-5-(2,4-dihydroxyphenyl)isoxazole

There total 1 articles about 3-<3,4-di(tert-butyldimethylsilyloxy)phenyl>-5-(2,4-dihydroxyphenyl)isoxazole 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:

: 41046-68-8
4-iodobenzene-1,3-diol

: 3-<3,4-di(tert-butyldimethylsilyloxy)phenyl>-5-tributylstannylisoxazole

: 169693-89-4
3-<3,4-di(tert-butyldimethylsilyloxy)phenyl>-5-(2,4-dihydroxyphenyl)isoxazole

Guidance literature:: With tris(dibenzylideneacetone)dipalladium ⁽⁰⁾; triphenyl-arsane; Yield given. Multistep reaction; 1.) dioxane, 10 min, 2.) 24 h, 50 deg C;

Reference yield: 98.0%

: 169693-89-4
3-<3,4-di(tert-butyldimethylsilyloxy)phenyl>-5-(2,4-dihydroxyphenyl)isoxazole

: 169693-93-0
3-(3,4-dihydroxyphenyl)-5-(2,4-dihydroxyphenyl)isoxazole

Guidance literature:: With potassium fluoride; sodium acetate; acetic acid; at 110 ℃; for 2h;

Reference yield:

: 169693-89-4
3-<3,4-di(tert-butyldimethylsilyloxy)phenyl>-5-(2,4-dihydroxyphenyl)isoxazole

: 2150-11-0
3',4',7-trihydroxyflavone

Guidance literature:: Multi-step reaction with 2 steps

1: 98 percent / HOAc, NaOAc, KF / 2 h / 110 °C

2: 1.) H₂, 2.) glacial acetic acid, conc. H₂SO₄ / 1.) Raney-Ni / 1.) methanol, 2.) 120 deg C, 2.5 h

With potassium fluoride; sulfuric acid; hydrogen; sodium acetate; acetic acid; nickel;