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2-naphthylmethyl O-(methyl 4-O-levulinoyl-β-D-glucopyranosyluronate)-(1->3)-4,6-O-benzylidene-2-deoxy-2-trichloroacetamido-β-D-galactopyranoside

Base Information
  • Chemical Name:2-naphthylmethyl O-(methyl 4-O-levulinoyl-β-D-glucopyranosyluronate)-(1->3)-4,6-O-benzylidene-2-deoxy-2-trichloroacetamido-β-D-galactopyranoside
  • CAS No.:890131-35-8
  • Molecular Formula:C38H40Cl3NO14
  • Molecular Weight:841.093
  • Hs Code.:
2-naphthylmethyl O-(methyl 4-O-levulinoyl-β-D-glucopyranosyluronate)-(1->3)-4,6-O-benzylidene-2-deoxy-2-trichloroacetamido-β-D-galactopyranoside

Synonyms:2-naphthylmethyl O-(methyl 4-O-levulinoyl-β-D-glucopyranosyluronate)-(1->3)-4,6-O-benzylidene-2-deoxy-2-trichloroacetamido-β-D-galactopyranoside

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Chemical Property of 2-naphthylmethyl O-(methyl 4-O-levulinoyl-β-D-glucopyranosyluronate)-(1->3)-4,6-O-benzylidene-2-deoxy-2-trichloroacetamido-β-D-galactopyranoside
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Technology Process of 2-naphthylmethyl O-(methyl 4-O-levulinoyl-β-D-glucopyranosyluronate)-(1->3)-4,6-O-benzylidene-2-deoxy-2-trichloroacetamido-β-D-galactopyranoside

There total 9 articles about 2-naphthylmethyl O-(methyl 4-O-levulinoyl-β-D-glucopyranosyluronate)-(1->3)-4,6-O-benzylidene-2-deoxy-2-trichloroacetamido-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:
Guidance literature:
Multi-step reaction with 7 steps
1: 89 percent / n-Bu4NBr; BF3*Et2O; TMSBr / 2,4,6-collidine / CH2Cl2 / 48 h / 20 °C
2: 90 percent / trimethylsilyl trifluoromethanesulfonate / CH2Cl2 / 0.5 h
3: NaOMe / methanol
4: trifluoroacetic acid / 4 h
5: 83 percent / camphorsulfonic acid / dimethylformamide / 1.5 h
6: 92 percent / N,N-dicyclohexylcarbodiimide; 4-dimethylaminopyridine / CH2Cl2 / 1 h
7: 79 percent / AcOH / CH2Cl2; H2O / 24 h / 20 °C
With dmap; trimethylsilyl bromide; trimethylsilyl trifluoromethanesulfonate; camphor-10-sulfonic acid; boron trifluoride diethyl etherate; tetrabutylammomium bromide; sodium methylate; acetic acid; dicyclohexyl-carbodiimide; trifluoroacetic acid; 2,4,6-trimethyl-pyridine; In methanol; dichloromethane; water; N,N-dimethyl-formamide;
DOI:10.1002/anie.200503551
Guidance literature:
Multi-step reaction with 6 steps
1: 90 percent / trimethylsilyl trifluoromethanesulfonate / CH2Cl2 / 0.5 h
2: NaOMe / methanol
3: trifluoroacetic acid / 4 h
4: 83 percent / camphorsulfonic acid / dimethylformamide / 1.5 h
5: 92 percent / N,N-dicyclohexylcarbodiimide; 4-dimethylaminopyridine / CH2Cl2 / 1 h
6: 79 percent / AcOH / CH2Cl2; H2O / 24 h / 20 °C
With dmap; trimethylsilyl trifluoromethanesulfonate; camphor-10-sulfonic acid; sodium methylate; acetic acid; dicyclohexyl-carbodiimide; trifluoroacetic acid; In methanol; dichloromethane; water; N,N-dimethyl-formamide;
DOI:10.1002/anie.200503551
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