(2S,3R,4S)-5-(tert-Butyl-dimethyl-silanyloxy)-3-(dimethyl-phenyl-silanyl)-2,4-dimethyl-pentanoic acid methyl ester

Base Information

Chemical Name:(2S,3R,4S)-5-(tert-Butyl-dimethyl-silanyloxy)-3-(dimethyl-phenyl-silanyl)-2,4-dimethyl-pentanoic acid methyl ester
CAS No.:97249-28-0
Molecular Formula:C₂₂H₄₀O₃Si₂
Molecular Weight:408.729
Hs Code.:

Synonyms:(2S,3R,4S)-5-(tert-Butyl-dimethyl-silanyloxy)-3-(dimethyl-phenyl-silanyl)-2,4-dimethyl-pentanoic acid methyl ester

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Chemical Property of (2S,3R,4S)-5-(tert-Butyl-dimethyl-silanyloxy)-3-(dimethyl-phenyl-silanyl)-2,4-dimethyl-pentanoic acid methyl ester

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Technology Process of (2S,3R,4S)-5-(tert-Butyl-dimethyl-silanyloxy)-3-(dimethyl-phenyl-silanyl)-2,4-dimethyl-pentanoic acid methyl ester

There total 9 articles about (2S,3R,4S)-5-(tert-Butyl-dimethyl-silanyloxy)-3-(dimethyl-phenyl-silanyl)-2,4-dimethyl-pentanoic acid methyl ester 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: 97.0%

: 97249-27-9
(3R,4R)-5-(tert-Butyl-dimethyl-silanyloxy)-3-(dimethyl-phenyl-silanyl)-4-methyl-pentanoic acid methyl ester

: 74-88-4
methyl iodide

: 97249-28-0
(2S,3R,4S)-5-(tert-Butyl-dimethyl-silanyloxy)-3-(dimethyl-phenyl-silanyl)-2,4-dimethyl-pentanoic acid methyl ester

Guidance literature:: With lithium diisopropyl amide; In tetrahydrofuran; 1.) -78 deg C, 10 min, 2.) r.t., 2 h;
DOI:10.1039/a804270e

Reference yield:

: 18162-48-6
tert-butyldimethylsilyl chloride

: 97249-28-0
(2S,3R,4S)-5-(tert-Butyl-dimethyl-silanyloxy)-3-(dimethyl-phenyl-silanyl)-2,4-dimethyl-pentanoic acid methyl ester

Guidance literature:: Multi-step reaction with 5 steps

1: imidazole / dimethylformamide / 8 h / 20 °C

2: 98 percent / p-TsOH / acetone / 6 h / 20 °C

3: KOH, AgNO₃ / aq. ethanol / 0.75 h / 0 °C

4: diethyl ether / 0.25 h / Ambient temperature

5: 97 percent / LDA / tetrahydrofuran / 1.) -78 deg C, 10 min, 2.) r.t., 2 h

With 1H-imidazole; potassium hydroxide; toluene-4-sulfonic acid; silver nitrate; lithium diisopropyl amide; In tetrahydrofuran; diethyl ether; ethanol; N,N-dimethyl-formamide; acetone;
DOI:10.1039/a804270e

Reference yield:

: 3-(Dimethyl-phenyl-silanyl)-5,5-dimethoxy-2-methyl-pentan-1-ol

: 97249-28-0
(2S,3R,4S)-5-(tert-Butyl-dimethyl-silanyloxy)-3-(dimethyl-phenyl-silanyl)-2,4-dimethyl-pentanoic acid methyl ester

Guidance literature:: Multi-step reaction with 5 steps

1: imidazole / dimethylformamide / 8 h / 20 °C

2: 98 percent / p-TsOH / acetone / 6 h / 20 °C

3: KOH, AgNO₃ / aq. ethanol / 0.75 h / 0 °C

4: diethyl ether / 0.25 h / Ambient temperature

5: 97 percent / LDA / tetrahydrofuran / 1.) -78 deg C, 10 min, 2.) r.t., 2 h

With 1H-imidazole; potassium hydroxide; toluene-4-sulfonic acid; silver nitrate; lithium diisopropyl amide; In tetrahydrofuran; diethyl ether; ethanol; N,N-dimethyl-formamide; acetone;
DOI:10.1039/a804270e