4-methoxy-2-methylphenyl 3,6-dideoxy-6-iodo-2-methoxy-3-phthalimido-α-D-glucopyranoside

Base Information

Chemical Name:4-methoxy-2-methylphenyl 3,6-dideoxy-6-iodo-2-methoxy-3-phthalimido-α-D-glucopyranoside
CAS No.:108512-33-0
Molecular Formula:C₂₃H₂₄INO₇
Molecular Weight:553.351
Hs Code.:

Synonyms:4-methoxy-2-methylphenyl 3,6-dideoxy-6-iodo-2-methoxy-3-phthalimido-α-D-glucopyranoside

Suppliers and Price of 4-methoxy-2-methylphenyl 3,6-dideoxy-6-iodo-2-methoxy-3-phthalimido-α-D-glucopyranoside

Supply Marketing:

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

Manufacturers and distributors:

Manufacture/Brand
Chemicals and raw materials
Packaging
price

Total 0 raw suppliers

Chemical Property of 4-methoxy-2-methylphenyl 3,6-dideoxy-6-iodo-2-methoxy-3-phthalimido-α-D-glucopyranoside

Chemical Property:

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:

Useful:

Technology Process of 4-methoxy-2-methylphenyl 3,6-dideoxy-6-iodo-2-methoxy-3-phthalimido-α-D-glucopyranoside

There total 13 articles about 4-methoxy-2-methylphenyl 3,6-dideoxy-6-iodo-2-methoxy-3-phthalimido-α-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: 97.0%

: 108512-32-9
4-methoxy-2-methylphenyl 3-deoxy-6-<(methylsulfonyl)oxy>-2-methoxy-3-phthalimido-α-D-glucopyranoside

: 108512-33-0
4-methoxy-2-methylphenyl 3,6-dideoxy-6-iodo-2-methoxy-3-phthalimido-α-D-glucopyranoside

Guidance literature:: With potassium iodide; In acetone; at 50 ℃; for 120h;
DOI:10.1021/jo00392a013

Reference yield:

: 4603-89-8
methyl 3-amino-4,6-O-benzylidene-3-deoxy-α-D-glucopyranoside

: 108512-33-0
4-methoxy-2-methylphenyl 3,6-dideoxy-6-iodo-2-methoxy-3-phthalimido-α-D-glucopyranoside

Guidance literature:: Multi-step reaction with 9 steps

1: 91 percent / triethylamine / dimethylsulfoxide / 16 h / 23 °C

2: 76 percent / Ag₂O / CH₂Cl₂ / 96 h / Heating

3: HOAc / 1 h / 100 °C

4: triethylamine, 4-(dimethylamino)pyridine / dimethylformamide / 15 h / 0 °C

5: 92 percent / conc. H₂SO₄ / acetic acid / 48 h / 23 °C

6: SnCl₄ / CH₂Cl₂ / 5 h / 23 °C

7: Dowex 2x8 / methanol / 0.5 h / Heating

8: 98 percent / pyridine / 48 h / 0 °C

9: 97 percent / KI / acetone / 120 h / 50 °C

With pyridine; dmap; Dowex 2x8; sulfuric acid; tin(IV) chloride; acetic acid; triethylamine; potassium iodide; silver(l) oxide; In methanol; dichloromethane; acetic acid; dimethyl sulfoxide; N,N-dimethyl-formamide; acetone;
DOI:10.1021/jo00392a013

Reference yield:

: 22509-74-6
N-ethoxycarbonylphthalimide

: 108512-33-0
4-methoxy-2-methylphenyl 3,6-dideoxy-6-iodo-2-methoxy-3-phthalimido-α-D-glucopyranoside

Guidance literature:: Multi-step reaction with 9 steps

1: 91 percent / triethylamine / dimethylsulfoxide / 16 h / 23 °C

2: 76 percent / Ag₂O / CH₂Cl₂ / 96 h / Heating

3: HOAc / 1 h / 100 °C

4: triethylamine, 4-(dimethylamino)pyridine / dimethylformamide / 15 h / 0 °C

5: 92 percent / conc. H₂SO₄ / acetic acid / 48 h / 23 °C

6: SnCl₄ / CH₂Cl₂ / 5 h / 23 °C

7: Dowex 2x8 / methanol / 0.5 h / Heating

8: 98 percent / pyridine / 48 h / 0 °C

9: 97 percent / KI / acetone / 120 h / 50 °C

With pyridine; dmap; Dowex 2x8; sulfuric acid; tin(IV) chloride; acetic acid; triethylamine; potassium iodide; silver(l) oxide; In methanol; dichloromethane; acetic acid; dimethyl sulfoxide; N,N-dimethyl-formamide; acetone;
DOI:10.1021/jo00392a013