Technology Process of octyl 6-O-<2-O-(3,4,6-tri-O-acetyl-2-deoxy-2-phthalimido-β-D-gluco-pyranosyl)-3,4,6-tri-O-benzyl-α-D-manno-pyranosyl>-4,8-anhydro-2,3-di-O-benzyl-7-deoxy-L-glycero-β-D-gluco-octopyranoside
There total 9 articles about octyl 6-O-<2-O-(3,4,6-tri-O-acetyl-2-deoxy-2-phthalimido-β-D-gluco-pyranosyl)-3,4,6-tri-O-benzyl-α-D-manno-pyranosyl>-4,8-anhydro-2,3-di-O-benzyl-7-deoxy-L-glycero-β-D-gluco-octopyranoside 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 3 steps
1: 86 percent / tetramethylurea, silver trifluoromethanesulfonate / CH2Cl2 / 0.5 h / Ambient temperature
2: sodium methoxide / methanol / 1 h / Ambient temperature
3: silver trifluoromethanesulfonate, 2,6-lutidine, molecular sieves (4A) / CH2Cl2 / 1.) -50 deg C, 30 min, 2.) RT, 1 h
With
2,6-dimethylpyridine; 4 A molecular sieve; sodium methylate; silver trifluoromethanesulfonate; tetramethylurea;
In
methanol; dichloromethane;
- Guidance literature:
-
Multi-step reaction with 7 steps
1: 78 percent / silver zeolite / CH2Cl2 / 2 h / Ambient temperature
2: 97 percent / sodium methoxide / methanol / Ambient temperature
3: 74 percent / 4-(N,N-dimethylamino)pyridine / CH2Cl2 / 1.) from 0 deg C to -18 deg C, 15 h, 2.) RT, 60 min
4: 63 percent / sodium hydride / dimethylformamide / 3 h / -50 - 20 °C
5: 86 percent / tetramethylurea, silver trifluoromethanesulfonate / CH2Cl2 / 0.5 h / Ambient temperature
6: sodium methoxide / methanol / 1 h / Ambient temperature
7: silver trifluoromethanesulfonate, 2,6-lutidine, molecular sieves (4A) / CH2Cl2 / 1.) -50 deg C, 30 min, 2.) RT, 1 h
With
2,6-dimethylpyridine; dmap; 4 A molecular sieve; silver zeolite; sodium methylate; silver trifluoromethanesulfonate; sodium hydride; tetramethylurea;
In
methanol; dichloromethane; N,N-dimethyl-formamide;
- Guidance literature:
-
Multi-step reaction with 5 steps
1: 74 percent / 4-(N,N-dimethylamino)pyridine / CH2Cl2 / 1.) from 0 deg C to -18 deg C, 15 h, 2.) RT, 60 min
2: 63 percent / sodium hydride / dimethylformamide / 3 h / -50 - 20 °C
3: 86 percent / tetramethylurea, silver trifluoromethanesulfonate / CH2Cl2 / 0.5 h / Ambient temperature
4: sodium methoxide / methanol / 1 h / Ambient temperature
5: silver trifluoromethanesulfonate, 2,6-lutidine, molecular sieves (4A) / CH2Cl2 / 1.) -50 deg C, 30 min, 2.) RT, 1 h
With
2,6-dimethylpyridine; dmap; 4 A molecular sieve; sodium methylate; silver trifluoromethanesulfonate; sodium hydride; tetramethylurea;
In
methanol; dichloromethane; N,N-dimethyl-formamide;