7-octen-1-yl 4-O-(4,6-O-benzylidene-3-O-pivaloyl-β-D-galactopyranosyl)-2,3,6-tri-O-benzyl-β-D-glucopyranoside

Base Information

Chemical Name:7-octen-1-yl 4-O-(4,6-O-benzylidene-3-O-pivaloyl-β-D-galactopyranosyl)-2,3,6-tri-O-benzyl-β-D-glucopyranoside
CAS No.:1192261-22-5
Molecular Formula:C₅₃H₆₆O₁₂
Molecular Weight:895.1
Hs Code.:

Synonyms:7-octen-1-yl 4-O-(4,6-O-benzylidene-3-O-pivaloyl-β-D-galactopyranosyl)-2,3,6-tri-O-benzyl-β-D-glucopyranoside

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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 7-octen-1-yl 4-O-(4,6-O-benzylidene-3-O-pivaloyl-β-D-galactopyranosyl)-2,3,6-tri-O-benzyl-β-D-glucopyranoside

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Technology Process of 7-octen-1-yl 4-O-(4,6-O-benzylidene-3-O-pivaloyl-β-D-galactopyranosyl)-2,3,6-tri-O-benzyl-β-D-glucopyranoside

There total 1 articles about 7-octen-1-yl 4-O-(4,6-O-benzylidene-3-O-pivaloyl-β-D-galactopyranosyl)-2,3,6-tri-O-benzyl-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: 95.0%

: 1192261-21-4
7-octen-1-yl 4-O-(4,6-O-benzylidene-β-D-galactopyranosyl)-2,3,6-tri-O-benzyl-β-D-glucopyranoside

: 3282-30-2
pivaloyl chloride

: 1192261-22-5
7-octen-1-yl 4-O-(4,6-O-benzylidene-3-O-pivaloyl-β-D-galactopyranosyl)-2,3,6-tri-O-benzyl-β-D-glucopyranoside

Guidance literature:: With pyridine; at 20 ℃;
DOI:10.1071/CH09058

Reference yield: 78.0%

: 1192261-22-5
7-octen-1-yl 4-O-(4,6-O-benzylidene-3-O-pivaloyl-β-D-galactopyranosyl)-2,3,6-tri-O-benzyl-β-D-glucopyranoside

: 136633-04-0
O-(2,3,4-tri-O-benzyl-α-L-fucopyranosyl) trichloroacetimidate

: 1229735-32-3
C₈₀H₉₄O₁₆

Guidance literature:: With trimethylsilyl trifluoromethanesulfonate; In diethyl ether; at -10 ℃; stereoselective reaction; Molecular sieve;
DOI:10.1071/CH09058