methyl 4,6-O-benzylidene-3-O-(2-chloroacetyl)-2-deoxy-2-phthalimido-β-D-glucopyranoside

Base Information

Chemical Name:methyl 4,6-O-benzylidene-3-O-(2-chloroacetyl)-2-deoxy-2-phthalimido-β-D-glucopyranoside
CAS No.:1214746-31-2
Molecular Formula:C₂₄H₂₂ClNO₈
Molecular Weight:487.894
Hs Code.:

Synonyms:methyl 4,6-O-benzylidene-3-O-(2-chloroacetyl)-2-deoxy-2-phthalimido-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 methyl 4,6-O-benzylidene-3-O-(2-chloroacetyl)-2-deoxy-2-phthalimido-β-D-glucopyranoside

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Technology Process of methyl 4,6-O-benzylidene-3-O-(2-chloroacetyl)-2-deoxy-2-phthalimido-β-D-glucopyranoside

There total 1 articles about methyl 4,6-O-benzylidene-3-O-(2-chloroacetyl)-2-deoxy-2-phthalimido-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: 84.0%

: 81927-56-2
methyl 4,6-O-benzylidene-2-deoxy-2-phthalimide-β-D-glucopyranoside

: 541-88-8
Chloroacetic anhydride

: 1214746-31-2
methyl 4,6-O-benzylidene-3-O-(2-chloroacetyl)-2-deoxy-2-phthalimido-β-D-glucopyranoside

Guidance literature:: With pyridine; at 0 ℃; for 3h; Inert atmosphere;
DOI:10.1021/jo9026098

Reference yield: 90.0%

: 1214746-31-2
methyl 4,6-O-benzylidene-3-O-(2-chloroacetyl)-2-deoxy-2-phthalimido-β-D-glucopyranoside

: 1214746-33-4
methyl 4-O-benzoyl-3-O-(2-chloroacetyl)-2-deoxy-2-phthalimido-β-D-glucopyranoside

: 1214746-32-3
methyl 6-O-benzoyl-3-O-(2-chloroacetyl)-2-deoxy-2-phthalimido-β-D-glucopyranoside

Guidance literature:: With 3,3-dimethyldioxirane; In acetone; at 5 ℃; for 96h; regioselective reaction; Inert atmosphere;
DOI:10.1021/jo9026098