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4-benzyloxy-5-benzyloxymethyl-2-<(3'-tetrahydropyranyloxymethyl)pentylidene>tetrahydropyran

Base Information
  • Chemical Name:4-benzyloxy-5-benzyloxymethyl-2-<(3'-tetrahydropyranyloxymethyl)pentylidene>tetrahydropyran
  • CAS No.:113195-27-0
  • Molecular Formula:C31H42O5
  • Molecular Weight:494.671
  • Hs Code.:
4-benzyloxy-5-benzyloxymethyl-2-<(3'-tetrahydropyranyloxymethyl)pentylidene>tetrahydropyran

Synonyms:

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Chemical Property of 4-benzyloxy-5-benzyloxymethyl-2-<(3'-tetrahydropyranyloxymethyl)pentylidene>tetrahydropyran
Chemical Property:
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Technology Process of 4-benzyloxy-5-benzyloxymethyl-2-<(3'-tetrahydropyranyloxymethyl)pentylidene>tetrahydropyran

There total 26 articles about 4-benzyloxy-5-benzyloxymethyl-2-<(3'-tetrahydropyranyloxymethyl)pentylidene>tetrahydropyran 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 16 steps
1: NaBH4 / methanol
2: p-TsOH*H2O / diethyl ether
3: LiAlH4 / diethyl ether
4: p-TsOH*H2O / methanol
5: 98.3 g / p-TsOH*H2O / acetone
6: 97 percent / pyridinium chlorochromate, MS (3 Angstroem) / CH2Cl2
7: 64 percent / p-TsOH*H2O / CH2Cl2 / Heating
8: 72 percent / pyridinium dichromate, MS (3 Angstroem) / CH2Cl2
9: 1.) LDA, HMPA, 2.) HMPA / 1.) hexane/THF, -76 -72 deg C, 13 min, then -35 deg C, 2.) -78 deg C, 15 min
10: 11 percent / sucrose, phosphate buffer, baker's yeast, 0.2 percent Triton -100 aq. / 1 h / 30 °C
11: p-TsOH*H2O / ethanol; H2O / 168 h / Ambient temperature
12: 4-(N,N-dimethylamino)pyridine / pyridine
13: 97 percent / LAH / diethyl ether
14: 80 percent / NaH (60 percent), n-Bu4N(1+)*I(1-) / paraffin; tetrahydrofuran / 1 h / Heating
15: acetonitrile / 1 h / Heating
16: 1.) HMPA, n-BuLi / 1.) THF/n-hexane, -67 deg C, 30 min, 2.) THF, -67 -63 deg C, then room temperature, 3 h 50 min and 6 h 15 min
With N,N,N,N,N,N-hexamethylphosphoric triamide; dmap; sodium tetrahydroborate; lithium aluminium tetrahydride; dipyridinium dichromate; n-butyllithium; baker's yeast; phosphate buffer; MS (3 Angstroem); Triton -100; tetra-(n-butyl)ammonium iodide; sodium hydride; toluene-4-sulfonic acid; pyridinium chlorochromate; lithium diisopropyl amide; Sucrose; toluene-4-sulfonic acid; In tetrahydrofuran; pyridine; methanol; diethyl ether; ethanol; dichloromethane; water; acetone; acetonitrile; paraffin;
DOI:10.1016/S0040-4020(01)89929-4
Guidance literature:
Multi-step reaction with 12 steps
1: 98.3 g / p-TsOH*H2O / acetone
2: 97 percent / pyridinium chlorochromate, MS (3 Angstroem) / CH2Cl2
3: 64 percent / p-TsOH*H2O / CH2Cl2 / Heating
4: 72 percent / pyridinium dichromate, MS (3 Angstroem) / CH2Cl2
5: 1.) LDA, HMPA, 2.) HMPA / 1.) hexane/THF, -76 -72 deg C, 13 min, then -35 deg C, 2.) -78 deg C, 15 min
6: 11 percent / sucrose, phosphate buffer, baker's yeast, 0.2 percent Triton -100 aq. / 1 h / 30 °C
7: p-TsOH*H2O / ethanol; H2O / 168 h / Ambient temperature
8: 4-(N,N-dimethylamino)pyridine / pyridine
9: 97 percent / LAH / diethyl ether
10: 80 percent / NaH (60 percent), n-Bu4N(1+)*I(1-) / paraffin; tetrahydrofuran / 1 h / Heating
11: acetonitrile / 1 h / Heating
12: 1.) HMPA, n-BuLi / 1.) THF/n-hexane, -67 deg C, 30 min, 2.) THF, -67 -63 deg C, then room temperature, 3 h 50 min and 6 h 15 min
With N,N,N,N,N,N-hexamethylphosphoric triamide; dmap; lithium aluminium tetrahydride; dipyridinium dichromate; n-butyllithium; baker's yeast; phosphate buffer; MS (3 Angstroem); Triton -100; tetra-(n-butyl)ammonium iodide; sodium hydride; pyridinium chlorochromate; lithium diisopropyl amide; Sucrose; toluene-4-sulfonic acid; In tetrahydrofuran; pyridine; diethyl ether; ethanol; dichloromethane; water; acetone; acetonitrile; paraffin;
DOI:10.1016/S0040-4020(01)89929-4
Guidance literature:
Multi-step reaction with 15 steps
1: p-TsOH*H2O / diethyl ether
2: LiAlH4 / diethyl ether
3: p-TsOH*H2O / methanol
4: 98.3 g / p-TsOH*H2O / acetone
5: 97 percent / pyridinium chlorochromate, MS (3 Angstroem) / CH2Cl2
6: 64 percent / p-TsOH*H2O / CH2Cl2 / Heating
7: 72 percent / pyridinium dichromate, MS (3 Angstroem) / CH2Cl2
8: 1.) LDA, HMPA, 2.) HMPA / 1.) hexane/THF, -76 -72 deg C, 13 min, then -35 deg C, 2.) -78 deg C, 15 min
9: 11 percent / sucrose, phosphate buffer, baker's yeast, 0.2 percent Triton -100 aq. / 1 h / 30 °C
10: p-TsOH*H2O / ethanol; H2O / 168 h / Ambient temperature
11: 4-(N,N-dimethylamino)pyridine / pyridine
12: 97 percent / LAH / diethyl ether
13: 80 percent / NaH (60 percent), n-Bu4N(1+)*I(1-) / paraffin; tetrahydrofuran / 1 h / Heating
14: acetonitrile / 1 h / Heating
15: 1.) HMPA, n-BuLi / 1.) THF/n-hexane, -67 deg C, 30 min, 2.) THF, -67 -63 deg C, then room temperature, 3 h 50 min and 6 h 15 min
With N,N,N,N,N,N-hexamethylphosphoric triamide; dmap; lithium aluminium tetrahydride; dipyridinium dichromate; n-butyllithium; baker's yeast; phosphate buffer; MS (3 Angstroem); Triton -100; tetra-(n-butyl)ammonium iodide; sodium hydride; toluene-4-sulfonic acid; pyridinium chlorochromate; lithium diisopropyl amide; Sucrose; toluene-4-sulfonic acid; In tetrahydrofuran; pyridine; methanol; diethyl ether; ethanol; dichloromethane; water; acetone; acetonitrile; paraffin;
DOI:10.1016/S0040-4020(01)89929-4
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