(5R,8R)-5,8-Bis<(tert-butyldimethylsilyl)oxy>-1,12-bis<(p-tolylsulfonyl)oxy>dodecane

Base Information

Chemical Name:(5R,8R)-5,8-Bis<(tert-butyldimethylsilyl)oxy>-1,12-bis<(p-tolylsulfonyl)oxy>dodecane
CAS No.:131618-51-4
Molecular Formula:C₃₈H₆₆O₈S₂Si₂
Molecular Weight:771.24
Hs Code.:

Synonyms:(5R,8R)-5,8-Bis<(tert-butyldimethylsilyl)oxy>-1,12-bis<(p-tolylsulfonyl)oxy>dodecane

Suppliers and Price of (5R,8R)-5,8-Bis<(tert-butyldimethylsilyl)oxy>-1,12-bis<(p-tolylsulfonyl)oxy>dodecane

Supply Marketing:

Business phase:: The product has achieved commercial mass production^*data from LookChem market partment

Manufacturers and distributors:

Manufacture/Brand
Chemicals and raw materials
Packaging
price

Total 0 raw suppliers

Chemical Property of (5R,8R)-5,8-Bis<(tert-butyldimethylsilyl)oxy>-1,12-bis<(p-tolylsulfonyl)oxy>dodecane

Chemical Property:

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:

Useful:

Technology Process of (5R,8R)-5,8-Bis<(tert-butyldimethylsilyl)oxy>-1,12-bis<(p-tolylsulfonyl)oxy>dodecane

There total 6 articles about (5R,8R)-5,8-Bis<(tert-butyldimethylsilyl)oxy>-1,12-bis<(p-tolylsulfonyl)oxy>dodecane 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: 83.0%

: 131618-30-9
(5R,8R)-5,8-Bis<(tert-butyldimethylsilyl)oxy>-1,12-dodecanediol

: 98-59-9
p-toluenesulfonyl chloride

: 131618-51-4
(5R,8R)-5,8-Bis<(tert-butyldimethylsilyl)oxy>-1,12-bis<(p-tolylsulfonyl)oxy>dodecane

Guidance literature:: With dmap;
DOI:10.1021/jo00004a011

Reference yield:

: 24211-51-6
(2S,5S)-hexane-1,2,5,6-tetrol

: 131618-51-4
(5R,8R)-5,8-Bis<(tert-butyldimethylsilyl)oxy>-1,12-bis<(p-tolylsulfonyl)oxy>dodecane

Guidance literature:: Multi-step reaction with 6 steps

1: pyridine / 1.) ice bath, 30 min, 2.) r.t., 1 h

2: 58 percent / 15percent NaOH / tetrahydrofuran / 1.5 h / Ambient temperature

3: 59 percent / CuI / tetrahydrofuran / 1.5 h / -15 °C

4: 88 percent / imidazole / dimethylformamide / 5 h / Ambient temperature

5: 90 percent / H₂ / 10percent Pd/C / methanol / 5 h

6: 83 percent / 4-(dimethylamino)pyridine

With pyridine; 1H-imidazole; dmap; sodium hydroxide; copper(l) iodide; hydrogen; palladium on activated charcoal; In tetrahydrofuran; methanol; N,N-dimethyl-formamide;
DOI:10.1021/jo00004a011

Reference yield:

: 74862-78-5
(2S,5S)-1,6-di-(p-toluenesulfonyloxy)-2,5-dihydroxy-hexane

: 131618-51-4
(5R,8R)-5,8-Bis<(tert-butyldimethylsilyl)oxy>-1,12-bis<(p-tolylsulfonyl)oxy>dodecane

Guidance literature:: Multi-step reaction with 5 steps

1: 58 percent / 15percent NaOH / tetrahydrofuran / 1.5 h / Ambient temperature

2: 59 percent / CuI / tetrahydrofuran / 1.5 h / -15 °C

3: 88 percent / imidazole / dimethylformamide / 5 h / Ambient temperature

4: 90 percent / H₂ / 10percent Pd/C / methanol / 5 h

5: 83 percent / 4-(dimethylamino)pyridine

With 1H-imidazole; dmap; sodium hydroxide; copper(l) iodide; hydrogen; palladium on activated charcoal; In tetrahydrofuran; methanol; N,N-dimethyl-formamide;
DOI:10.1021/jo00004a011