4-methoxyphenyl 2,3-di-O-benzoyl-4,6-O-benzylidene-β-D-galactopyranoside

Base Information

Chemical Name:4-methoxyphenyl 2,3-di-O-benzoyl-4,6-O-benzylidene-β-D-galactopyranoside
CAS No.:176165-20-1
Molecular Formula:C₃₄H₃₀O₉
Molecular Weight:582.607
Hs Code.:

Synonyms:4-methoxyphenyl 2,3-di-O-benzoyl-4,6-O-benzylidene-β-D-galactopyranoside

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

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Chemical Property of 4-methoxyphenyl 2,3-di-O-benzoyl-4,6-O-benzylidene-β-D-galactopyranoside

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Technology Process of 4-methoxyphenyl 2,3-di-O-benzoyl-4,6-O-benzylidene-β-D-galactopyranoside

There total 1 articles about 4-methoxyphenyl 2,3-di-O-benzoyl-4,6-O-benzylidene-β-D-galactopyranoside 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: 92.0%

: 98-88-4
benzoyl chloride

: 176299-96-0
4-methoxyphenyl 4,6-O-benzylidene-β-D-galactopyranoside

: 176165-20-1
4-methoxyphenyl 2,3-di-O-benzoyl-4,6-O-benzylidene-β-D-galactopyranoside

Guidance literature:: With pyridine; at 0 ℃; for 1h;
DOI:10.1016/j.carres.2003.10.012

Reference yield: 93.0%

: 176165-20-1
4-methoxyphenyl 2,3-di-O-benzoyl-4,6-O-benzylidene-β-D-galactopyranoside

: 1053380-04-3
p-methoxyphenyl 2,3-di-O-benzoyl-β-D-galactopyranoside

Guidance literature:: With acetic acid; In water; at 85 ℃; for 2h;
DOI:10.1016/j.tetasy.2010.09.002

Reference yield: 88.0%

: 176165-20-1
4-methoxyphenyl 2,3-di-O-benzoyl-4,6-O-benzylidene-β-D-galactopyranoside

: 176165-21-2
p-methoxyphenyl 2,3-di-O-benzoyl-6-O-benzyl-β-D-galactopyranoside

Guidance literature:: With triethylsilane; iodine; In acetonitrile; at 0 - 5 ℃; for 0.416667h; regioselective reaction;
DOI:10.1055/s-0029-1219798