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[(1R,6S,10R)-1-(3-Methoxy-phenyl)-bicyclo[4.3.1]dec-10-yl]-methyl-amine

Base Information
  • Chemical Name:[(1R,6S,10R)-1-(3-Methoxy-phenyl)-bicyclo[4.3.1]dec-10-yl]-methyl-amine
  • CAS No.:75209-85-7
  • Molecular Formula:C18H27NO
  • Molecular Weight:273.418
  • Hs Code.:
[(1R,6S,10R)-1-(3-Methoxy-phenyl)-bicyclo[4.3.1]dec-10-yl]-methyl-amine

Synonyms:

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Chemical Property of [(1R,6S,10R)-1-(3-Methoxy-phenyl)-bicyclo[4.3.1]dec-10-yl]-methyl-amine
Chemical Property:
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Technology Process of [(1R,6S,10R)-1-(3-Methoxy-phenyl)-bicyclo[4.3.1]dec-10-yl]-methyl-amine

There total 26 articles about [(1R,6S,10R)-1-(3-Methoxy-phenyl)-bicyclo[4.3.1]dec-10-yl]-methyl-amine 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 13 steps
1: 1.) Mg / 1.) THF, 2.) THF, room temp., 30 min, 50-55 deg C, 1 h
2: oxalic acid / toluene / 16 h / Heating
3: 1.) NaBH4, BF3*Et2O, 2.) 10percent NaOH, 30percent H2O2 / 1.) THF, room temp., 15 h, 2.) THF, H2O, room temp., 1 h
4: 33.6 percent / Na2Cr2O7*2H2O, conc. H2SO4 / diethyl ether; H2O / 2 h / 5 - 13 °C
5: 75.8 percent / TiCl4 / benzene / 1.) room temp., overnight, 2.) 75-80 deg C, 8 h
6: 78 percent / benzene / 20 h / Heating
7: 90.3 percent / NH2OH*HCl, NaOAc / dimethylformamide / Ambient temperature
8: 81.9 percent / LiAlH4 / tetrahydrofuran; dioxane / Heating
9: 73.3 percent / 5percent NaHCO3 / CH2Cl2 / 4 h / Ambient temperature
10: 80.2 percent / pyridine / 4 h / Ambient temperature
11: 44.3 percent / NaI, Zn / 1,2-dimethoxy-ethane / 76 h / Heating
12: 97.7 percent / H2 / 10percent Pd-C / ethanol / 7.5 h / 70 - 90 °C / 47808 Torr
13: LiAlH4 / diethyl ether / 8 h / Heating
With sodium hydroxide; sodium tetrahydroborate; lithium aluminium tetrahydride; sodium dichromate; sulfuric acid; boron trifluoride diethyl etherate; hydroxylamine hydrochloride; hydrogen; dihydrogen peroxide; sodium acetate; oxalic acid; titanium tetrachloride; sodium hydrogencarbonate; magnesium; sodium iodide; zinc; palladium on activated charcoal; In tetrahydrofuran; 1,4-dioxane; pyridine; 1,2-dimethoxyethane; diethyl ether; ethanol; dichloromethane; water; N,N-dimethyl-formamide; toluene; benzene;
DOI:10.1248/cpb.28.1022
Guidance literature:
Multi-step reaction with 13 steps
1: 1.) Mg / 1.) THF, 2.) THF, room temp., 30 min, 50-55 deg C, 1 h
2: oxalic acid / toluene / 16 h / Heating
3: 1.) NaBH4, BF3*Et2O, 2.) 10percent NaOH, 30percent H2O2 / 1.) THF, room temp., 15 h, 2.) THF, H2O, room temp., 1 h
4: 33.6 percent / Na2Cr2O7*2H2O, conc. H2SO4 / diethyl ether; H2O / 2 h / 5 - 13 °C
5: 75.8 percent / TiCl4 / benzene / 1.) room temp., overnight, 2.) 75-80 deg C, 8 h
6: 78 percent / benzene / 20 h / Heating
7: 90.3 percent / NH2OH*HCl, NaOAc / dimethylformamide / Ambient temperature
8: 81.9 percent / LiAlH4 / tetrahydrofuran; dioxane / Heating
9: 73.3 percent / 5percent NaHCO3 / CH2Cl2 / 4 h / Ambient temperature
10: 80.2 percent / pyridine / 4 h / Ambient temperature
11: 44.3 percent / NaI, Zn / 1,2-dimethoxy-ethane / 76 h / Heating
12: 97.7 percent / H2 / 10percent Pd-C / ethanol / 7.5 h / 70 - 90 °C / 47808 Torr
13: LiAlH4 / tetrahydrofuran / 18 h / Heating
With sodium hydroxide; sodium tetrahydroborate; lithium aluminium tetrahydride; sodium dichromate; sulfuric acid; boron trifluoride diethyl etherate; hydroxylamine hydrochloride; hydrogen; dihydrogen peroxide; sodium acetate; oxalic acid; titanium tetrachloride; sodium hydrogencarbonate; magnesium; sodium iodide; zinc; palladium on activated charcoal; In tetrahydrofuran; 1,4-dioxane; pyridine; 1,2-dimethoxyethane; diethyl ether; ethanol; dichloromethane; water; N,N-dimethyl-formamide; toluene; benzene;
DOI:10.1248/cpb.28.1022
Guidance literature:
Multi-step reaction with 12 steps
1: oxalic acid / toluene / 16 h / Heating
2: 1.) NaBH4, BF3*Et2O, 2.) 10percent NaOH, 30percent H2O2 / 1.) THF, room temp., 15 h, 2.) THF, H2O, room temp., 1 h
3: 33.6 percent / Na2Cr2O7*2H2O, conc. H2SO4 / diethyl ether; H2O / 2 h / 5 - 13 °C
4: 75.8 percent / TiCl4 / benzene / 1.) room temp., overnight, 2.) 75-80 deg C, 8 h
5: 78 percent / benzene / 20 h / Heating
6: 90.3 percent / NH2OH*HCl, NaOAc / dimethylformamide / Ambient temperature
7: 81.9 percent / LiAlH4 / tetrahydrofuran; dioxane / Heating
8: 73.3 percent / 5percent NaHCO3 / CH2Cl2 / 4 h / Ambient temperature
9: 80.2 percent / pyridine / 4 h / Ambient temperature
10: 44.3 percent / NaI, Zn / 1,2-dimethoxy-ethane / 76 h / Heating
11: 97.7 percent / H2 / 10percent Pd-C / ethanol / 7.5 h / 70 - 90 °C / 47808 Torr
12: LiAlH4 / diethyl ether / 8 h / Heating
With sodium hydroxide; sodium tetrahydroborate; lithium aluminium tetrahydride; sodium dichromate; sulfuric acid; boron trifluoride diethyl etherate; hydroxylamine hydrochloride; hydrogen; dihydrogen peroxide; sodium acetate; oxalic acid; titanium tetrachloride; sodium hydrogencarbonate; sodium iodide; zinc; palladium on activated charcoal; In tetrahydrofuran; 1,4-dioxane; pyridine; 1,2-dimethoxyethane; diethyl ether; ethanol; dichloromethane; water; N,N-dimethyl-formamide; toluene; benzene;
DOI:10.1248/cpb.28.1022
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