ethyl 3-O-allyl-2-O-benzyl-4,6-O-benzylidene-1-thio-β-D-galactopyranoside

Base Information

Chemical Name:ethyl 3-O-allyl-2-O-benzyl-4,6-O-benzylidene-1-thio-β-D-galactopyranoside
CAS No.:1203549-89-6
Molecular Formula:C₂₅H₃₀O₅S
Molecular Weight:442.576
Hs Code.:

Synonyms:ethyl 3-O-allyl-2-O-benzyl-4,6-O-benzylidene-1-thio-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 ethyl 3-O-allyl-2-O-benzyl-4,6-O-benzylidene-1-thio-β-D-galactopyranoside

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Technology Process of ethyl 3-O-allyl-2-O-benzyl-4,6-O-benzylidene-1-thio-β-D-galactopyranoside

There total 1 articles about ethyl 3-O-allyl-2-O-benzyl-4,6-O-benzylidene-1-thio-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:

: 100-39-0
benzyl bromide

: ethyl 3-O-allyl-4,6-O-benzylidene-1-thio-β-D-galactopyranoside

: 1203549-89-6
ethyl 3-O-allyl-2-O-benzyl-4,6-O-benzylidene-1-thio-β-D-galactopyranoside

Guidance literature:: With tetrabutylammomium bromide; sodium hydroxide; In tetrahydrofuran; at 20 ℃; for 4h;
DOI:10.1080/07328300903261554

Reference yield: 89.0%

: 1064679-21-5
4-methoxyphenyl (4-O-acetyl-2,6-di-O-benzyl-β-D-galactopyranosyl)-(1->4)-2,3,6-tri-O-benzyl-β-D-glucopyranoside

: 1203549-89-6
ethyl 3-O-allyl-2-O-benzyl-4,6-O-benzylidene-1-thio-β-D-galactopyranoside

: 1203549-91-0
4-methoxyphenyl (3-O-allyl-2-O-benzyl-4,6-O-benzylidene-α-D-galactopyranosyl)-(1->3)-(4-O-acetyl-2,6-di-O-benzyl-β-D-galactopyranosyl)-(1->4)-2,3,6-tri-O-benzyl-β-D-glucopyranoside

Guidance literature:: With N-iodo-succinimide; trimethylsilyl trifluoromethanesulfonate; In dichloromethane; at -40 ℃; for 1h; stereoselective reaction; Inert atmosphere; Molecular sieve;
DOI:10.1080/07328300903261554