(1-O-(tert-butyldimethylsilyl)-3,4,6-tri-O-benzyl-α-D-fructofuranosyl)methyl benzoate

Base Information

Chemical Name:(1-O-(tert-butyldimethylsilyl)-3,4,6-tri-O-benzyl-α-D-fructofuranosyl)methyl benzoate
CAS No.:111085-88-2
Molecular Formula:C₄₁H₅₀O₇Si
Molecular Weight:682.929
Hs Code.:

Synonyms:(1-O-(tert-butyldimethylsilyl)-3,4,6-tri-O-benzyl-α-D-fructofuranosyl)methyl benzoate

Suppliers and Price of (1-O-(tert-butyldimethylsilyl)-3,4,6-tri-O-benzyl-α-D-fructofuranosyl)methyl benzoate

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 (1-O-(tert-butyldimethylsilyl)-3,4,6-tri-O-benzyl-α-D-fructofuranosyl)methyl benzoate

Chemical Property:

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:

Useful:

Technology Process of (1-O-(tert-butyldimethylsilyl)-3,4,6-tri-O-benzyl-α-D-fructofuranosyl)methyl benzoate

There total 7 articles about (1-O-(tert-butyldimethylsilyl)-3,4,6-tri-O-benzyl-α-D-fructofuranosyl)methyl benzoate 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: 84.0%

: 98-88-4
benzoyl chloride

: 111085-93-9
1-(1-O-(tert-butyldimethylsilyl)-3,4,6-tri-O-benzyl-α-D-fructofuranosyl)methanol

: 111085-88-2
(1-O-(tert-butyldimethylsilyl)-3,4,6-tri-O-benzyl-α-D-fructofuranosyl)methyl benzoate

Guidance literature:: With pyridine; In dichloromethane; for 2h; Ambient temperature;
DOI:10.1021/jo00234a024

Reference yield:

: 18162-48-6
tert-butyldimethylsilyl chloride

: 111085-88-2
(1-O-(tert-butyldimethylsilyl)-3,4,6-tri-O-benzyl-α-D-fructofuranosyl)methyl benzoate

Guidance literature:: Multi-step reaction with 4 steps

1: 90 percent / Et₃N, (dimethylamino)pyridine / CH₂Cl₂ / 96 h / Ambient temperature

2: 92 percent / PdCl₂(CH₃CN)2 / benzene / Heating

3: 1.) O₃, PPh₃, 2.) Zn(BH₄)2 / 1.) CH₂Cl₂, from -78 deg C to RT, 2.) Et₂O, overnight

4: 84 percent / pyridine / CH₂Cl₂ / 2 h / Ambient temperature

With pyridine; dmap; dichloro bis(acetonitrile) palladium(II); zinc(II) tetrahydroborate; ozone; triethylamine; triphenylphosphine; In dichloromethane; benzene;
DOI:10.1021/jo00234a024

Reference yield:

: 111085-83-7
1-(3,4,6-tri-O-benzyl-α-D-fructofuranosyl)-2-propene

: 111085-88-2
(1-O-(tert-butyldimethylsilyl)-3,4,6-tri-O-benzyl-α-D-fructofuranosyl)methyl benzoate

Guidance literature:: Multi-step reaction with 4 steps

1: 90 percent / Et₃N, (dimethylamino)pyridine / CH₂Cl₂ / 96 h / Ambient temperature

2: 92 percent / PdCl₂(CH₃CN)2 / benzene / Heating

3: 1.) O₃, PPh₃, 2.) Zn(BH₄)2 / 1.) CH₂Cl₂, from -78 deg C to RT, 2.) Et₂O, overnight

4: 84 percent / pyridine / CH₂Cl₂ / 2 h / Ambient temperature

With pyridine; dmap; dichloro bis(acetonitrile) palladium(II); zinc(II) tetrahydroborate; ozone; triethylamine; triphenylphosphine; In dichloromethane; benzene;
DOI:10.1021/jo00234a024