(4R,5S)-5-[(2R,4R)-5-(tert-butyldiphenylsilyloxy)-4-(triethylsilyloxy)pent-2-yl]-2,2-dimethyl-1,3-dioxolane-4-carboxylic acid ethyl ester

Base Information

• Chemical Name: (4R,5S)-5-[(2R,4R)-5-(tert-butyldiphenylsilyloxy)-4-(triethylsilyloxy)pent-2-yl]-2,2-dimethyl-1,3-dioxolane-4-carboxylic acid ethyl ester
• CAS No.: 922516-87-8
• Molecular Formula: C₃₅H₅₆O₆Si₂
• Molecular Weight: 628.997
• Mol file: 922516-87-8.mol

Synonyms:(4R,5S)-5-[(2R,4R)-5-(tert-butyldiphenylsilyloxy)-4-(triethylsilyloxy)pent-2-yl]-2,2-dimethyl-1,3-dioxolane-4-carboxylic acid ethyl ester

Chemical Property of (4R,5S)-5-[(2R,4R)-5-(tert-butyldiphenylsilyloxy)-4-(triethylsilyloxy)pent-2-yl]-2,2-dimethyl-1,3-dioxolane-4-carboxylic acid ethyl ester

Chemical Property:

Purity/Quality:

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

Useful:

Technology Process of (4R,5S)-5-[(2R,4R)-5-(tert-butyldiphenylsilyloxy)-4-(triethylsilyloxy)pent-2-yl]-2,2-dimethyl-1,3-dioxolane-4-carboxylic acid ethyl ester

There total 2 articles about (4R,5S)-5-[(2R,4R)-5-(tert-butyldiphenylsilyloxy)-4-(triethylsilyloxy)pent-2-yl]-2,2-dimethyl-1,3-dioxolane-4-carboxylic acid ethyl 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%

(4R,5S)-5-[(2R,4R)-5-(tert-butyldiphenylsilyloxy)-4-hydroxypent-2-yl]-2,2-dimethyl-1,3-dioxolane-4-carboxylic acid ethyl ester (922516-86-7) + triethylsilyl trifluoromethyl sulfonate (79271-56-0) → (4R,5S)-5-[(2R,4R)-5-(tert-butyldiphenylsilyloxy)-4-(triethylsilyloxy)pent-2-yl]-2,2-dimethyl-1,3-dioxolane-4-carboxylic acid ethyl ester (922516-87-8)

Guidance literature:

With 2,6-dimethylpyridine; In dichloromethane; at 20 ℃; for 1h;

DOI:10.1016/j.tetasy.2006.10.024

Reference yield:

(2R,3S,4R,6R)-7-(tert-butyldiphenylsilyloxy)-2,3,6-trihydroxy-4-methylheptanoic acid ethyl ester (922516-85-6) → (4R,5S)-5-[(2R,4R)-5-(tert-butyldiphenylsilyloxy)-4-(triethylsilyloxy)pent-2-yl]-2,2-dimethyl-1,3-dioxolane-4-carboxylic acid ethyl ester (922516-87-8)

Guidance literature:

Multi-step reaction with 2 steps

1: 76 percent / camphorsulfonic acid; molecular sieves 3 Angstroem / acetone / 18 h / 20 °C

2: 97 percent / 2,6-lutidine / CH₂Cl₂ / 1 h / 20 °C

With 2,6-dimethylpyridine; 3 A molecular sieve; camphor-10-sulfonic acid; In dichloromethane; acetone;

DOI:10.1016/j.tetasy.2006.10.024

Reference yield:

(4R,5S)-5-[(2R,4R)-5-(tert-butyldiphenylsilyloxy)-4-(triethylsilyloxy)pent-2-yl]-2,2-dimethyl-1,3-dioxolane-4-carboxylic acid ethyl ester (922516-87-8) → (4R,5S)-5-[(1R,3R)-4-(tert-Butyl-diphenyl-silanyloxy)-1-methyl-3-triethylsilanyloxy-butyl]-2,2-dimethyl-[1,3]dioxolane-4-carboxylic acid

Guidance literature:

With potassium trimethylsilonate; In tetrahydrofuran; at 20 ℃; for 1h;

DOI:10.1016/j.tetasy.2006.10.024

upstream raw materials:

(4R,5S)-5-[(2R,4R)-5-(tert-butyldiphenylsilyloxy)-4-hydroxypent-2-yl]-2,2-dimethyl-1,3-dioxolane-4-carboxylic acid ethyl ester

triethylsilyl trifluoromethyl sulfonate

(2R,3S,4R,6R)-7-(tert-butyldiphenylsilyloxy)-2,3,6-trihydroxy-4-methylheptanoic acid ethyl ester

Downstream raw materials:

(4R,5S)-5-[(2R,4R)-5-(tert-butyldiphenylsilyloxy)-4-(triethylsilyloxy)pent-2-yl]-2,2-dimethyl-1,3-dioxolane-4-carboxylic acid N-methoxy-N-methylamide