(R)-1-[2-(tert-Butyl-dimethyl-silanyloxymethyl)-phenyl]-ethane-1,2-diol

Base Information

Chemical Name:(R)-1-[2-(tert-Butyl-dimethyl-silanyloxymethyl)-phenyl]-ethane-1,2-diol
CAS No.:159143-38-1
Molecular Formula:C₁₅H₂₆O₃Si
Molecular Weight:282.455
Hs Code.:

Synonyms:(R)-1-[2-(tert-Butyl-dimethyl-silanyloxymethyl)-phenyl]-ethane-1,2-diol

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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 (R)-1-[2-(tert-Butyl-dimethyl-silanyloxymethyl)-phenyl]-ethane-1,2-diol

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Technology Process of (R)-1-[2-(tert-Butyl-dimethyl-silanyloxymethyl)-phenyl]-ethane-1,2-diol

There total 6 articles about (R)-1-[2-(tert-Butyl-dimethyl-silanyloxymethyl)-phenyl]-ethane-1,2-diol 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:

: 5159-41-1
2-iodobenzyl alcohol

: 159143-38-1
(R)-1-[2-(tert-Butyl-dimethyl-silanyloxymethyl)-phenyl]-ethane-1,2-diol

Guidance literature:: Multi-step reaction with 5 steps

1: 1.) Ph₃P, diethylamine, 2.) PdCl₂, CuI / 1) 25 deg C, 30 min; 2) 0-5 deg C, 2 h

2: 93 percent / imidazole / CH₂Cl₂ / 2 h / Ambient temperature

3: 96 percent / NaOH / benzene / 3.5 h / Heating

4: 89 percent / H₂, quinoline / Lindlar's catalyst / hexane / 3.5 h / Ambient temperature

5: AD-mix-β / 2-methyl-propan-2-ol; H2O / 20 h / 0 °C

With 1H-imidazole; quinoline; sodium hydroxide; copper(l) iodide; AD-mix-β; hydrogen; diethylamine; triphenylphosphine; palladium dichloride; Lindlar's catalyst; In hexane; dichloromethane; water; tert-butyl alcohol; benzene;
DOI:10.1021/jo9519367

Reference yield:

: 18162-48-6
tert-butyldimethylsilyl chloride

: 159143-38-1
(R)-1-[2-(tert-Butyl-dimethyl-silanyloxymethyl)-phenyl]-ethane-1,2-diol

Guidance literature:: Multi-step reaction with 4 steps

1: 93 percent / imidazole / CH₂Cl₂ / 2 h / Ambient temperature

2: 96 percent / NaOH / benzene / 3.5 h / Heating

3: 89 percent / H₂, quinoline / Lindlar's catalyst / hexane / 3.5 h / Ambient temperature

4: AD-mix-β / 2-methyl-propan-2-ol; H2O / 20 h / 0 °C

With 1H-imidazole; quinoline; sodium hydroxide; AD-mix-β; hydrogen; Lindlar's catalyst; In hexane; dichloromethane; water; tert-butyl alcohol; benzene;
DOI:10.1021/jo9519367

Reference yield:

: 159143-37-0
2-methyl-4-<2-<<(tert-butyldimethylsilyl)oxy>methyl>phenyl>-3-butyn-2-ol

: 159143-38-1
(R)-1-[2-(tert-Butyl-dimethyl-silanyloxymethyl)-phenyl]-ethane-1,2-diol

Guidance literature:: Multi-step reaction with 3 steps

1: 96 percent / NaOH / benzene / 3.5 h / Heating

2: 89 percent / H₂, quinoline / Lindlar's catalyst / hexane / 3.5 h / Ambient temperature

3: AD-mix-β / 2-methyl-propan-2-ol; H2O / 20 h / 0 °C

With quinoline; sodium hydroxide; AD-mix-β; hydrogen; Lindlar's catalyst; In hexane; water; tert-butyl alcohol; benzene;
DOI:10.1021/jo9519367