(2E,6E)-8-[t-butyl(diphenyl)silyl]oxy-2,6-dimethyl-2,6-octadienyl-1,1-d₂ 1-methanesulfonate

Base Information

• Chemical Name: (2E,6E)-8-[t-butyl(diphenyl)silyl]oxy-2,6-dimethyl-2,6-octadienyl-1,1-d₂ 1-methanesulfonate
• CAS No.: 916754-53-5
• Molecular Formula: C₂₇H₃₈O₄SSi
• Molecular Weight: 488.732

Synonyms:(2E,6E)-8-[t-butyl(diphenyl)silyl]oxy-2,6-dimethyl-2,6-octadienyl-1,1-d₂ 1-methanesulfonate

Chemical Property of (2E,6E)-8-[t-butyl(diphenyl)silyl]oxy-2,6-dimethyl-2,6-octadienyl-1,1-d₂ 1-methanesulfonate

Chemical Property:

Purity/Quality:

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

Useful:

Technology Process of (2E,6E)-8-[t-butyl(diphenyl)silyl]oxy-2,6-dimethyl-2,6-octadienyl-1,1-d₂ 1-methanesulfonate

There total 7 articles about (2E,6E)-8-[t-butyl(diphenyl)silyl]oxy-2,6-dimethyl-2,6-octadienyl-1,1-d₂ 1-methanesulfonate 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:

(2E,6E)-8-[t-butyl(diphenyl)silyl]oxy-2,6-dimethyl-2,6-octadien-1-ol-1,1-d2 (916754-49-9) + methanesulfonyl chloride (124-63-0) → (2E,6E)-8-[t-butyl(diphenyl)silyl]oxy-2,6-dimethyl-2,6-octadienyl-1,1-d2 1-methanesulfonate (916754-53-5)

Guidance literature:

With triethylamine; In dichloromethane; at 0 ℃; for 0.75h;

DOI:10.1002/ejoc.200600367

Reference yield:

methyl (2E,6E)-8-[t-butyl(diphenyl)silyl]oxy-2,6-dimethyl-2,6-octadienoate (916754-48-8) → (2E,6E)-8-[t-butyl(diphenyl)silyl]oxy-2,6-dimethyl-2,6-octadienyl-1,1-d2 1-methanesulfonate (916754-53-5)

Guidance literature:

Multi-step reaction with 2 steps

1: 65 percent / LiAlD₄ / diethyl ether / 0.5 h / 0 °C

2: triethylamine / CH₂Cl₂ / 0.75 h / 0 °C

With lithium aluminium deuteride; triethylamine; In diethyl ether; dichloromethane;

DOI:10.1002/ejoc.200600367

Reference yield:

Geraniol (106-24-1) → (2E,6E)-8-[t-butyl(diphenyl)silyl]oxy-2,6-dimethyl-2,6-octadienyl-1,1-d2 1-methanesulfonate (916754-53-5)

Guidance literature:

Multi-step reaction with 6 steps

1: 100 percent / imidazole / dimethylformamide / 1 h / 20 °C

2: 70 percent / MCPBA / CHCl₃ / 1 h / 0 °C

3: HIO₄*2H₂O / tetrahydrofuran; diethyl ether / 1 h / 0 °C

4: 7.0 g / CH₂Cl₂ / 3 h / 20 °C

5: 65 percent / LiAlD₄ / diethyl ether / 0.5 h / 0 °C

6: triethylamine / CH₂Cl₂ / 0.75 h / 0 °C

With 1H-imidazole; lithium aluminium deuteride; periodic acid; triethylamine; 3-chloro-benzenecarboperoxoic acid; In tetrahydrofuran; diethyl ether; dichloromethane; chloroform; N,N-dimethyl-formamide;

DOI:10.1002/ejoc.200600367

upstream raw materials:

(2E,6E)-8-[t-butyl(diphenyl)silyl]oxy-2,6-dimethyl-2,6-octadien-1-ol-1,1-d₂

methanesulfonyl chloride

methyl (2E,6E)-8-[t-butyl(diphenyl)silyl]oxy-2,6-dimethyl-2,6-octadienoate

Geraniol

Downstream raw materials:

(E,E)-1-t-butyldiphenylsilyloxy-3,7-dimethyl-2,6-octadiene-8,8,8-d₃

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