benzyl endo-3,4-O-benzylidene-2-O-(p-toluenesulfonyl)-β-L-arabinopyranoside

Base Information

Chemical Name:benzyl endo-3,4-O-benzylidene-2-O-(p-toluenesulfonyl)-β-L-arabinopyranoside
CAS No.:81704-66-7
Molecular Formula:C₂₆H₂₆O₇S
Molecular Weight:482.554
Hs Code.:

Synonyms:benzyl endo-3,4-O-benzylidene-2-O-(p-toluenesulfonyl)-β-L-arabinopyranoside

Suppliers and Price of benzyl endo-3,4-O-benzylidene-2-O-(p-toluenesulfonyl)-β-L-arabinopyranoside

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 benzyl endo-3,4-O-benzylidene-2-O-(p-toluenesulfonyl)-β-L-arabinopyranoside

Chemical Property:

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:

Useful:

Technology Process of benzyl endo-3,4-O-benzylidene-2-O-(p-toluenesulfonyl)-β-L-arabinopyranoside

There total 3 articles about benzyl endo-3,4-O-benzylidene-2-O-(p-toluenesulfonyl)-β-L-arabinopyranoside 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: 87.4%

: 79936-12-2
benzyl endo-3,4-O-benzylidene-β-L-arabinopyranoside

: 98-59-9
p-toluenesulfonyl chloride

: 81704-66-7
benzyl endo-3,4-O-benzylidene-2-O-(p-toluenesulfonyl)-β-L-arabinopyranoside

Guidance literature:: In pyridine; 1 h, 0 deg C, room t., 90 h;

Reference yield:

: 1125-88-8
benzaldehyde dimethyl acetal

: 81704-66-7
benzyl endo-3,4-O-benzylidene-2-O-(p-toluenesulfonyl)-β-L-arabinopyranoside

Guidance literature:: Multi-step reaction with 2 steps

1: 15.9 percent / p-toluene sulfonic acid / dimethylformamide / 3 h / 60 °C / in vacuum

2: 87.4 percent / pyridine / 1 h, 0 deg C, room t., 90 h

toluene-4-sulfonic acid; In pyridine; N,N-dimethyl-formamide;

Reference yield:

: 7473-38-3
benzyl β-L-arabinopyranoside

: 81704-66-7
benzyl endo-3,4-O-benzylidene-2-O-(p-toluenesulfonyl)-β-L-arabinopyranoside

Guidance literature:: Multi-step reaction with 2 steps

1: 15.9 percent / p-toluene sulfonic acid / dimethylformamide / 3 h / 60 °C / in vacuum

2: 87.4 percent / pyridine / 1 h, 0 deg C, room t., 90 h

toluene-4-sulfonic acid; In pyridine; N,N-dimethyl-formamide;