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1-((3aR,7R,7aR)-7-Fluoro-4,4-diphenyl-octahydro-isoindol-2-yl)-2-[2-(3-pyrrolidin-1-yl-propoxy)-phenyl]-ethanone

Base Information Edit
  • Chemical Name:1-((3aR,7R,7aR)-7-Fluoro-4,4-diphenyl-octahydro-isoindol-2-yl)-2-[2-(3-pyrrolidin-1-yl-propoxy)-phenyl]-ethanone
  • CAS No.:146402-84-8
  • Molecular Formula:C35H41FN2O2
  • Molecular Weight:540.721
  • Hs Code.:
  • Mol file:146402-84-8.mol
1-((3aR,7R,7aR)-7-Fluoro-4,4-diphenyl-octahydro-isoindol-2-yl)-2-[2-(3-pyrrolidin-1-yl-propoxy)-phenyl]-ethanone

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Suppliers and Price of 1-((3aR,7R,7aR)-7-Fluoro-4,4-diphenyl-octahydro-isoindol-2-yl)-2-[2-(3-pyrrolidin-1-yl-propoxy)-phenyl]-ethanone
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The product has achieved commercial mass production*data from LookChem market partment
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Chemical Property of 1-((3aR,7R,7aR)-7-Fluoro-4,4-diphenyl-octahydro-isoindol-2-yl)-2-[2-(3-pyrrolidin-1-yl-propoxy)-phenyl]-ethanone Edit
Chemical Property:
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Technology Process of 1-((3aR,7R,7aR)-7-Fluoro-4,4-diphenyl-octahydro-isoindol-2-yl)-2-[2-(3-pyrrolidin-1-yl-propoxy)-phenyl]-ethanone

There total 8 articles about 1-((3aR,7R,7aR)-7-Fluoro-4,4-diphenyl-octahydro-isoindol-2-yl)-2-[2-(3-pyrrolidin-1-yl-propoxy)-phenyl]-ethanone 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 9 steps
1: 98 percent / t-BuOK / various solvent(s) / 20 °C
2: PTSA / toluene
3: Red-Al / toluene / 0 - 20 °C
4: 70 percent / CF3COOH / toluene / 35 °C
5: H2 / Pd/C (5percent) / butan-1-ol; acetic acid / 20 °C
6: 1.) NaBH4 / 1.) aq. NaOH / 1.) MeOH, -20 deg C; 2.) MeOH
7: 90 percent / n-perfluorobutanesulfonyl fluoride, diethylamine / tetrahydrofuran / 20 °C
8: conc. HCl / propan-2-ol / 60 °C
9: SOCl2 / CH2Cl2
With hydrogenchloride; sodium tetrahydroborate; thionyl chloride; Nonafluorobutanesulfonyl fluoride; potassium tert-butylate; hydrogen; diethylamine; sodium bis(2-methoxyethoxy)aluminium dihydride; sodium hydroxide; palladium on activated charcoal; toluene-4-sulfonic acid; trifluoroacetic acid; In tetrahydrofuran; dichloromethane; acetic acid; isopropyl alcohol; toluene; butan-1-ol;
DOI:10.1016/0040-4039(96)01760-1
Guidance literature:
Multi-step reaction with 6 steps
1: 70 percent / CF3COOH / toluene / 35 °C
2: H2 / Pd/C (5percent) / butan-1-ol; acetic acid / 20 °C
3: 1.) NaBH4 / 1.) aq. NaOH / 1.) MeOH, -20 deg C; 2.) MeOH
4: 90 percent / n-perfluorobutanesulfonyl fluoride, diethylamine / tetrahydrofuran / 20 °C
5: conc. HCl / propan-2-ol / 60 °C
6: SOCl2 / CH2Cl2
With hydrogenchloride; sodium tetrahydroborate; thionyl chloride; Nonafluorobutanesulfonyl fluoride; hydrogen; diethylamine; sodium hydroxide; palladium on activated charcoal; trifluoroacetic acid; In tetrahydrofuran; dichloromethane; acetic acid; isopropyl alcohol; toluene; butan-1-ol;
DOI:10.1016/0040-4039(96)01760-1
Guidance literature:
Multi-step reaction with 8 steps
1: PTSA / toluene
2: Red-Al / toluene / 0 - 20 °C
3: 70 percent / CF3COOH / toluene / 35 °C
4: H2 / Pd/C (5percent) / butan-1-ol; acetic acid / 20 °C
5: 1.) NaBH4 / 1.) aq. NaOH / 1.) MeOH, -20 deg C; 2.) MeOH
6: 90 percent / n-perfluorobutanesulfonyl fluoride, diethylamine / tetrahydrofuran / 20 °C
7: conc. HCl / propan-2-ol / 60 °C
8: SOCl2 / CH2Cl2
With hydrogenchloride; sodium tetrahydroborate; thionyl chloride; Nonafluorobutanesulfonyl fluoride; hydrogen; diethylamine; sodium bis(2-methoxyethoxy)aluminium dihydride; sodium hydroxide; palladium on activated charcoal; toluene-4-sulfonic acid; trifluoroacetic acid; In tetrahydrofuran; dichloromethane; acetic acid; isopropyl alcohol; toluene; butan-1-ol;
DOI:10.1016/0040-4039(96)01760-1
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