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2-Piperidinone, 6-[2-(2-bromo-4,5-dimethoxyphenyl)-2-oxoethyl]-1-[(2S)-2-[(phenylmeth oxy)methyl]-1-pyrrolidinyl]-, (6R)-

Base Information Edit
  • Chemical Name:2-Piperidinone, 6-[2-(2-bromo-4,5-dimethoxyphenyl)-2-oxoethyl]-1-[(2S)-2-[(phenylmeth oxy)methyl]-1-pyrrolidinyl]-, (6R)-
  • CAS No.:162756-00-5
  • Molecular Formula:C27H33BrN2O5
  • Molecular Weight:545.473
  • Hs Code.:
  • Mol file:162756-00-5.mol
2-Piperidinone,
6-[2-(2-bromo-4,5-dimethoxyphenyl)-2-oxoethyl]-1-[(2S)-2-[(phenylmeth
oxy)methyl]-1-pyrrolidinyl]-, (6R)-

Synonyms:

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The product has achieved commercial mass production*data from LookChem market partment
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Chemical Property of 2-Piperidinone, 6-[2-(2-bromo-4,5-dimethoxyphenyl)-2-oxoethyl]-1-[(2S)-2-[(phenylmeth oxy)methyl]-1-pyrrolidinyl]-, (6R)- Edit
Chemical Property:
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SDS file from LookChem

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Technology Process of 2-Piperidinone, 6-[2-(2-bromo-4,5-dimethoxyphenyl)-2-oxoethyl]-1-[(2S)-2-[(phenylmeth oxy)methyl]-1-pyrrolidinyl]-, (6R)-

There total 10 articles about 2-Piperidinone, 6-[2-(2-bromo-4,5-dimethoxyphenyl)-2-oxoethyl]-1-[(2S)-2-[(phenylmeth oxy)methyl]-1-pyrrolidinyl]-, (6R)- 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 6 steps
1: 94 percent / NaH / tetrahydrofuran; dimethylformamide / 1.) room temp., 30 min, 2.) room temp., 3 h
2: LiAlH4 / tetrahydrofuran / 1.) room temp., 15 min, 2.) reflux, 2 h
3: 2.) Ac2O, NaOAc / 1.) CH2Cl2, room temp., 1 h, 2.) reflux, 1 h
4: 80 percent / LiEt3BH / tetrahydrofuran / 2 h / -78 °C
5: 80 percent / pyridinium p-toluenesulfonate / 3 h / Ambient temperature
6: 70 percent / BF3*Et2O / CH2Cl2 / 1 h / Ambient temperature
With lithium aluminium tetrahydride; boron trifluoride diethyl etherate; sodium acetate; pyridinium p-toluenesulfonate; acetic anhydride; sodium hydride; lithium triethylborohydride; In tetrahydrofuran; dichloromethane; N,N-dimethyl-formamide;
DOI:10.1021/jo00124a025
Guidance literature:
Multi-step reaction with 6 steps
1: 94 percent / NaH / tetrahydrofuran; dimethylformamide / 1.) room temp., 30 min, 2.) room temp., 3 h
2: LiAlH4 / tetrahydrofuran / 1.) room temp., 15 min, 2.) reflux, 2 h
3: 2.) Ac2O, NaOAc / 1.) CH2Cl2, room temp., 1 h, 2.) reflux, 1 h
4: 80 percent / LiEt3BH / tetrahydrofuran / 2 h / -78 °C
5: 80 percent / pyridinium p-toluenesulfonate / 3 h / Ambient temperature
6: 70 percent / BF3*Et2O / CH2Cl2 / 1 h / Ambient temperature
With lithium aluminium tetrahydride; boron trifluoride diethyl etherate; sodium acetate; pyridinium p-toluenesulfonate; acetic anhydride; sodium hydride; lithium triethylborohydride; In tetrahydrofuran; dichloromethane; N,N-dimethyl-formamide;
DOI:10.1021/jo00124a025
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