[(S)-3-((1R,2R)-3-Benzyloxy-1,2-dimethyl-propyl)-3-methyl-cyclohexyloxy]-tert-butyl-diphenyl-silane

Base Information

Chemical Name:[(S)-3-((1R,2R)-3-Benzyloxy-1,2-dimethyl-propyl)-3-methyl-cyclohexyloxy]-tert-butyl-diphenyl-silane
CAS No.:248916-41-8
Molecular Formula:C₃₅H₄₈O₂Si
Molecular Weight:528.85
Hs Code.:

Synonyms:[(S)-3-((1R,2R)-3-Benzyloxy-1,2-dimethyl-propyl)-3-methyl-cyclohexyloxy]-tert-butyl-diphenyl-silane

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Chemical Property of [(S)-3-((1R,2R)-3-Benzyloxy-1,2-dimethyl-propyl)-3-methyl-cyclohexyloxy]-tert-butyl-diphenyl-silane

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Technology Process of [(S)-3-((1R,2R)-3-Benzyloxy-1,2-dimethyl-propyl)-3-methyl-cyclohexyloxy]-tert-butyl-diphenyl-silane

There total 5 articles about [(S)-3-((1R,2R)-3-Benzyloxy-1,2-dimethyl-propyl)-3-methyl-cyclohexyloxy]-tert-butyl-diphenyl-silane 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: 90.0%

: 58479-61-1
tert-butylchlorodiphenylsilane

: 248916-40-7
(S)-3-((1R,2R)-3-Benzyloxy-1,2-dimethyl-propyl)-3-methyl-cyclohexanol

: 248916-41-8
[(S)-3-((1R,2R)-3-Benzyloxy-1,2-dimethyl-propyl)-3-methyl-cyclohexyloxy]-tert-butyl-diphenyl-silane

Guidance literature:: With 1H-imidazole; dmap; In N,N-dimethyl-formamide; at 20 ℃; for 16h;
DOI:10.1021/jm980736v

Reference yield:

: 248916-39-4
benzyl (2R,3R)-2-methyl-3-((1S)-1-methyl-2-cyclohexenyl)butyl ether

: 248916-41-8
[(S)-3-((1R,2R)-3-Benzyloxy-1,2-dimethyl-propyl)-3-methyl-cyclohexyloxy]-tert-butyl-diphenyl-silane

Guidance literature:: Multi-step reaction with 2 steps

1.1: 9-BBN / tetrahydrofuran / 48 h / Heating

1.2: 95 percent / 30 percent H₂O₂; 6 N aq. NaOH / ethanol / 1.5 h / 55 °C

2.1: 90 percent / imidazole; DMAP / dimethylformamide / 16 h / 20 °C

With 1H-imidazole; dmap; 9-borabicyclo[3.3.1]nonane dimer; In tetrahydrofuran; N,N-dimethyl-formamide; 1.1: hydroboration / 1.2: Oxidation / 2.1: silylation;
DOI:10.1021/jm980736v

Reference yield:

: (2R/S,3R)-4-benzyloxy-3-methyl-2-((1S)-1-methyl-2-cyclohexenyl)butanoic acid

: 248916-41-8
[(S)-3-((1R,2R)-3-Benzyloxy-1,2-dimethyl-propyl)-3-methyl-cyclohexyloxy]-tert-butyl-diphenyl-silane

Guidance literature:: Multi-step reaction with 5 steps

1.1: LiAlH₄ / tetrahydrofuran / 43 h / Heating

2.1: 97 percent / pyridine / 24 h / 0 °C

3.1: 94 percent / LiAlH₄ / tetrahydrofuran / 4 h / Heating

4.1: 9-BBN / tetrahydrofuran / 48 h / Heating

4.2: 95 percent / 30 percent H₂O₂; 6 N aq. NaOH / ethanol / 1.5 h / 55 °C

5.1: 90 percent / imidazole; DMAP / dimethylformamide / 16 h / 20 °C

With pyridine; 1H-imidazole; dmap; lithium aluminium tetrahydride; 9-borabicyclo[3.3.1]nonane dimer; In tetrahydrofuran; N,N-dimethyl-formamide; 1.1: Reduction / 2.1: Tosylation / 3.1: reductive cleavae / 4.1: hydroboration / 4.2: Oxidation / 5.1: silylation;
DOI:10.1021/jm980736v