(2S)-2-[(S)-(3,5-dimethoxy-4-methylphenyl){[dimethyl(2-methyl-2-propanyl)silyl]oxy}methyl]-5-phenyl-1-pentanol

Base Information

Chemical Name:(2S)-2-[(S)-(3,5-dimethoxy-4-methylphenyl){[dimethyl(2-methyl-2-propanyl)silyl]oxy}methyl]-5-phenyl-1-pentanol
CAS No.:856687-71-3
Molecular Formula:C₂₇H₄₂O₄Si
Molecular Weight:458.714
Hs Code.:

Synonyms:(2S)-2-[(S)-(3,5-dimethoxy-4-methylphenyl){[dimethyl(2-methyl-2-propanyl)silyl]oxy}methyl]-5-phenyl-1-pentanol

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Chemical Property of (2S)-2-[(S)-(3,5-dimethoxy-4-methylphenyl){[dimethyl(2-methyl-2-propanyl)silyl]oxy}methyl]-5-phenyl-1-pentanol

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Technology Process of (2S)-2-[(S)-(3,5-dimethoxy-4-methylphenyl){[dimethyl(2-methyl-2-propanyl)silyl]oxy}methyl]-5-phenyl-1-pentanol

There total 4 articles about (2S)-2-[(S)-(3,5-dimethoxy-4-methylphenyl){[dimethyl(2-methyl-2-propanyl)silyl]oxy}methyl]-5-phenyl-1-pentanol 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: 23.0%

: 856687-69-9
(4S)-4-benzyl-3-{(2R)-2-[(S)-(3,5-dimethoxy-4-methylphenyl){[dimethyl(2-methyl-2-propanyl)silyl]oxy}methyl]-5-phenylpentanoyl}-1,3-oxazolidin-2-one

: 856687-71-3
(2S)-2-[(S)-(3,5-dimethoxy-4-methylphenyl){[dimethyl(2-methyl-2-propanyl)silyl]oxy}methyl]-5-phenyl-1-pentanol

Guidance literature:: With lithium borohydride; In tetrahydrofuran; water; at 0 - 20 ℃; for 3h; Inert atmosphere;
DOI:10.1021/acsmedchemlett.7b00383

Reference yield:

: 1011-27-4
3,5-dimethoxy-4-methylbenzaldehyde

: 856687-71-3
(2S)-2-[(S)-(3,5-dimethoxy-4-methylphenyl){[dimethyl(2-methyl-2-propanyl)silyl]oxy}methyl]-5-phenyl-1-pentanol

Guidance literature:: Multi-step reaction with 3 steps

1.1: triethylamine; chloro-trimethyl-silane; magnesium chloride / ethyl acetate / 20 °C

1.2: 0.08 h

2.1: 2,6-dimethylpyridine / dichloromethane / 2 h / 0 °C

3.1: lithium borohydride / tetrahydrofuran; water / 3 h / 0 - 20 °C / Inert atmosphere

With 2,6-dimethylpyridine; lithium borohydride; chloro-trimethyl-silane; triethylamine; magnesium chloride; In tetrahydrofuran; dichloromethane; water; ethyl acetate;
DOI:10.1021/acsmedchemlett.7b00383

Reference yield:

: 161725-13-9
(4S)-4-benzyl-3-(5-phenylpentanoyl)-1,3-oxazolidin-2-one

: 856687-71-3
(2S)-2-[(S)-(3,5-dimethoxy-4-methylphenyl){[dimethyl(2-methyl-2-propanyl)silyl]oxy}methyl]-5-phenyl-1-pentanol

Guidance literature:: Multi-step reaction with 3 steps

1.1: triethylamine; chloro-trimethyl-silane; magnesium chloride / ethyl acetate / 20 °C

1.2: 0.08 h

2.1: 2,6-dimethylpyridine / dichloromethane / 2 h / 0 °C

3.1: lithium borohydride / tetrahydrofuran; water / 3 h / 0 - 20 °C / Inert atmosphere

With 2,6-dimethylpyridine; lithium borohydride; chloro-trimethyl-silane; triethylamine; magnesium chloride; In tetrahydrofuran; dichloromethane; water; ethyl acetate;
DOI:10.1021/acsmedchemlett.7b00383