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(benzyloxy-4 dimethoxy-3,5 phenyl)-1-r bis-hydroxymethyl-2-t, 3-c benzyloxy-7 methoxy-6 tetrahydro-1,2,3,4 naphtalene

Base Information Edit
  • Chemical Name:(benzyloxy-4 dimethoxy-3,5 phenyl)-1-r bis-hydroxymethyl-2-t, 3-c benzyloxy-7 methoxy-6 tetrahydro-1,2,3,4 naphtalene
  • CAS No.:92831-80-6
  • Molecular Formula:C35H38O7
  • Molecular Weight:570.683
  • Hs Code.:
  • Mol file:92831-80-6.mol
(benzyloxy-4 dimethoxy-3,5 phenyl)-1-r bis-hydroxymethyl-2-t, 3-c benzyloxy-7 methoxy-6 tetrahydro-1,2,3,4 naphtalene

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Chemical Property of (benzyloxy-4 dimethoxy-3,5 phenyl)-1-r bis-hydroxymethyl-2-t, 3-c benzyloxy-7 methoxy-6 tetrahydro-1,2,3,4 naphtalene Edit
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Technology Process of (benzyloxy-4 dimethoxy-3,5 phenyl)-1-r bis-hydroxymethyl-2-t, 3-c benzyloxy-7 methoxy-6 tetrahydro-1,2,3,4 naphtalene

There total 10 articles about (benzyloxy-4 dimethoxy-3,5 phenyl)-1-r bis-hydroxymethyl-2-t, 3-c benzyloxy-7 methoxy-6 tetrahydro-1,2,3,4 naphtalene 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 8 steps
1: 73 percent / methylate de sodium / 7 h / Heating
2: 66.5 percent / chlorure de calcium, borohydrure de sodium / ethanol; aq. KOH / 1.) room temperature, 5 h; 2.) 0 deg C, pH=1 (HCl 6N); 3.) -20 deg C
3: 77.6 percent / H2 / Pd/C (10percent) / ethyl acetate / 7 h / 3750.3 Torr / Ambient temperature
4: 93.6 percent / carbonate de potassium, iodure de sodium / acetone / 15 h / Heating
5: 92 percent / hexamethyldisilylamidure de lithium / benzene; hexane / 1.) 0 to -20 deg C
6: 52 percent / H2 / Pd/C (10percent) / ethyl acetate; trifluoroacetic acid / 4 h / 3750.3 Torr / Ambient temperature
7: 66.6 percent / carbonate de potassium, iodure de sodium / acetone / Heating
8: 1.) AlLiH4; 2.) H2O / 1.) THF, 30 min, 15 deg C to room temperature; 2.) THF
With sodium tetrahydroborate; lithium aluminium tetrahydride; chlorure de calcium; water; hydrogen; sodium methylate; potassium carbonate; sodium iodide; lithium hexamethyldisilazane; palladium on activated charcoal; In potassium hydroxide; ethanol; hexane; ethyl acetate; acetone; trifluoroacetic acid; benzene;
Guidance literature:
Multi-step reaction with 5 steps
1: 93.6 percent / carbonate de potassium, iodure de sodium / acetone / 15 h / Heating
2: 92 percent / hexamethyldisilylamidure de lithium / benzene; hexane / 1.) 0 to -20 deg C
3: 52 percent / H2 / Pd/C (10percent) / ethyl acetate; trifluoroacetic acid / 4 h / 3750.3 Torr / Ambient temperature
4: 66.6 percent / carbonate de potassium, iodure de sodium / acetone / Heating
5: 1.) AlLiH4; 2.) H2O / 1.) THF, 30 min, 15 deg C to room temperature; 2.) THF
With lithium aluminium tetrahydride; water; hydrogen; potassium carbonate; sodium iodide; lithium hexamethyldisilazane; palladium on activated charcoal; In hexane; ethyl acetate; acetone; trifluoroacetic acid; benzene;
Guidance literature:
Multi-step reaction with 4 steps
1: 92 percent / hexamethyldisilylamidure de lithium / benzene; hexane / 1.) 0 to -20 deg C
2: 52 percent / H2 / Pd/C (10percent) / ethyl acetate; trifluoroacetic acid / 4 h / 3750.3 Torr / Ambient temperature
3: 66.6 percent / carbonate de potassium, iodure de sodium / acetone / Heating
4: 1.) AlLiH4; 2.) H2O / 1.) THF, 30 min, 15 deg C to room temperature; 2.) THF
With lithium aluminium tetrahydride; water; hydrogen; potassium carbonate; sodium iodide; lithium hexamethyldisilazane; palladium on activated charcoal; In hexane; ethyl acetate; acetone; trifluoroacetic acid; benzene;
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