p-tolyl 4,6-di-O-benzyl-3-O-tert-butyldimethylsilyl-2-deoxy-2-phthalimido-1-thio-β-D-glucopyranoside

Base Information

Chemical Name:p-tolyl 4,6-di-O-benzyl-3-O-tert-butyldimethylsilyl-2-deoxy-2-phthalimido-1-thio-β-D-glucopyranoside
CAS No.:905266-85-5
Molecular Formula:C₄₁H₄₇NO₆SSi
Molecular Weight:709.979
Hs Code.:

Synonyms:p-tolyl 4,6-di-O-benzyl-3-O-tert-butyldimethylsilyl-2-deoxy-2-phthalimido-1-thio-β-D-glucopyranoside

Suppliers and Price of p-tolyl 4,6-di-O-benzyl-3-O-tert-butyldimethylsilyl-2-deoxy-2-phthalimido-1-thio-β-D-glucopyranoside

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 p-tolyl 4,6-di-O-benzyl-3-O-tert-butyldimethylsilyl-2-deoxy-2-phthalimido-1-thio-β-D-glucopyranoside

Chemical Property:

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:

Useful:

Technology Process of p-tolyl 4,6-di-O-benzyl-3-O-tert-butyldimethylsilyl-2-deoxy-2-phthalimido-1-thio-β-D-glucopyranoside

There total 4 articles about p-tolyl 4,6-di-O-benzyl-3-O-tert-butyldimethylsilyl-2-deoxy-2-phthalimido-1-thio-β-D-glucopyranoside 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:

: 909795-60-4
p-tolyl 2-deoxy-2-N-phthalimido-3-O-tert-butyldimethylsilyl-4-O-benzyl-1-thio-β-D-glucopyranoside

: 100-39-0
benzyl bromide

: 905266-85-5
p-tolyl 4,6-di-O-benzyl-3-O-tert-butyldimethylsilyl-2-deoxy-2-phthalimido-1-thio-β-D-glucopyranoside

Guidance literature:: With 4 A molecular sieve; tetra-(n-butyl)ammonium iodide; sodium hydride; In N,N-dimethyl-formamide; at 0 - 20 ℃; for 2h;
DOI:10.1016/j.carres.2006.01.007

Reference yield:

: 905266-84-4
p-tolyl 4,6-O-benzylidene-3-O-tert-butyldimethylsilyl-2-deoxy-2-phthalimido-1-thio-β-D-glucopyranoside

: 905266-85-5
p-tolyl 4,6-di-O-benzyl-3-O-tert-butyldimethylsilyl-2-deoxy-2-phthalimido-1-thio-β-D-glucopyranoside

Guidance literature:: Multi-step reaction with 2 steps

1: 0.39 g / BH₃*THF; trimethylsiyl triflate / CH₂Cl₂ / 4 h / -20 - 0 °C

2: 0.32 g / NaH; tetrabutylammonium iodide; 4 Angstroem molecular sieves / dimethylformamide / 2 h / 0 - 20 °C

With borane-THF; trimethylsilyl trifluoromethanesulfonate; 4 A molecular sieve; tetra-(n-butyl)ammonium iodide; sodium hydride; In dichloromethane; N,N-dimethyl-formamide;
DOI:10.1016/j.carres.2006.01.007

Reference yield:

: 69739-34-0
t-butyldimethylsiyl triflate

: 905266-85-5
p-tolyl 4,6-di-O-benzyl-3-O-tert-butyldimethylsilyl-2-deoxy-2-phthalimido-1-thio-β-D-glucopyranoside

Guidance literature:: Multi-step reaction with 3 steps

1: 85 percent / 4 Angstroem molecular sieves; 2,6 lutidine / CH₂Cl₂ / 4 h / 0 °C

2: 0.39 g / BH₃*THF; trimethylsiyl triflate / CH₂Cl₂ / 4 h / -20 - 0 °C

3: 0.32 g / NaH; tetrabutylammonium iodide; 4 Angstroem molecular sieves / dimethylformamide / 2 h / 0 - 20 °C

With 2,6-dimethylpyridine; borane-THF; trimethylsilyl trifluoromethanesulfonate; 4 A molecular sieve; tetra-(n-butyl)ammonium iodide; sodium hydride; In dichloromethane; N,N-dimethyl-formamide;
DOI:10.1016/j.carres.2006.01.007