(S)-2-(2-(4-(tert-butyldimethylsilyloxy)phenoxy)-5-iodophenyl)propan-1-ol

Base Information

Chemical Name:(S)-2-(2-(4-(tert-butyldimethylsilyloxy)phenoxy)-5-iodophenyl)propan-1-ol
CAS No.:924708-53-2
Molecular Formula:C₂₁H₂₉IO₃Si
Molecular Weight:484.449
Hs Code.:

Synonyms:(S)-2-(2-(4-(tert-butyldimethylsilyloxy)phenoxy)-5-iodophenyl)propan-1-ol

Suppliers and Price of (S)-2-(2-(4-(tert-butyldimethylsilyloxy)phenoxy)-5-iodophenyl)propan-1-ol

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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 (S)-2-(2-(4-(tert-butyldimethylsilyloxy)phenoxy)-5-iodophenyl)propan-1-ol

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Technology Process of (S)-2-(2-(4-(tert-butyldimethylsilyloxy)phenoxy)-5-iodophenyl)propan-1-ol

There total 6 articles about (S)-2-(2-(4-(tert-butyldimethylsilyloxy)phenoxy)-5-iodophenyl)propan-1-ol 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: 70.0%

: 924708-51-0
(R)-tert-butyl(4-(4-iodo-2-(oxiran-2-yl)phenoxy)phenoxy)dimethylsilane

: 917-54-4
methyllithium

: 924708-53-2
(S)-2-(2-(4-(tert-butyldimethylsilyloxy)phenoxy)-5-iodophenyl)propan-1-ol

Guidance literature:: With boron trifluoride diethyl etherate; copper(l) cyanide; In tetrahydrofuran; at -80 ℃;
DOI:10.1016/j.tet.2010.06.048

Reference yield:

: 924708-48-5
4-iodo-2-ethenylphenol

: 924708-53-2
(S)-2-(2-(4-(tert-butyldimethylsilyloxy)phenoxy)-5-iodophenyl)propan-1-ol

Guidance literature:: Multi-step reaction with 5 steps

1.1: 67 percent / copper(II) acetate; triethylamine / CH₂Cl₂ / 24 h / 20 °C

2.1: AD-mix-β / 2-methyl-propan-2-ol; H2O / 5 h / 0 °C

3.1: dibutyltin oxide; triethylamine / CH₂Cl₂ / 5 h / 20 °C

4.1: potassium tert-butoxide / tetrahydrofuran / 1 h / 0 °C

5.1: copper(I) cyanide / tetrahydrofuran / 0.5 h / -40 °C

5.2: BF₃*OEt₂ / tetrahydrofuran / 2 h / -80 °C

With AD-mix-β; potassium tert-butylate; copper diacetate; copper(l) cyanide; di(n-butyl)tin oxide; triethylamine; In tetrahydrofuran; dichloromethane; water; tert-butyl alcohol; 2.1: Sharpless asymmetric dihydroxylation;
DOI:10.1021/jo061980u

Reference yield:

: 924708-49-6
tert-butyl(4-(4-iodo-2-vinylphenoxy)phenoxy)dimethylsilane

: 924708-53-2
(S)-2-(2-(4-(tert-butyldimethylsilyloxy)phenoxy)-5-iodophenyl)propan-1-ol

Guidance literature:: Multi-step reaction with 4 steps

1.1: AD-mix-β / 2-methyl-propan-2-ol; H2O / 5 h / 0 °C

2.1: dibutyltin oxide; triethylamine / CH₂Cl₂ / 5 h / 20 °C

3.1: potassium tert-butoxide / tetrahydrofuran / 1 h / 0 °C

4.1: copper(I) cyanide / tetrahydrofuran / 0.5 h / -40 °C

4.2: BF₃*OEt₂ / tetrahydrofuran / 2 h / -80 °C

With AD-mix-β; potassium tert-butylate; copper(l) cyanide; di(n-butyl)tin oxide; triethylamine; In tetrahydrofuran; dichloromethane; water; tert-butyl alcohol; 1.1: Sharpless asymmetric dihydroxylation;
DOI:10.1021/jo061980u