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5-((3-bromo-2,6-dimethoxybenzamide)methyl)-5-hydroxy-1-ethyl-2-pyrrolidone

Base Information Edit
  • Chemical Name:5-((3-bromo-2,6-dimethoxybenzamide)methyl)-5-hydroxy-1-ethyl-2-pyrrolidone
  • CAS No.:125558-30-7
  • Molecular Formula:C16H21 Br N2 O5
  • Molecular Weight:401.25
  • Hs Code.:
  • Mol file:125558-30-7.mol
5-((3-bromo-2,6-dimethoxybenzamide)methyl)-5-hydroxy-1-ethyl-2-pyrrolidone

Synonyms:NCM 001

Suppliers and Price of 5-((3-bromo-2,6-dimethoxybenzamide)methyl)-5-hydroxy-1-ethyl-2-pyrrolidone
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The product has achieved commercial mass production*data from LookChem market partment
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Chemical Property of 5-((3-bromo-2,6-dimethoxybenzamide)methyl)-5-hydroxy-1-ethyl-2-pyrrolidone Edit
Chemical Property:
  • Vapor Pressure:6.72E-13mmHg at 25°C 
  • Boiling Point:549.3°Cat760mmHg 
  • PKA:12.31±0.20(Predicted) 
  • Flash Point:286°C 
  • PSA:88.10000 
  • Density:1.436g/cm3 
  • LogP:1.85580 
Purity/Quality:
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MSDS Files:

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Technology Process of 5-((3-bromo-2,6-dimethoxybenzamide)methyl)-5-hydroxy-1-ethyl-2-pyrrolidone

There total 13 articles about 5-((3-bromo-2,6-dimethoxybenzamide)methyl)-5-hydroxy-1-ethyl-2-pyrrolidone 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: SOCl2, N,N-dimethylformamide / toluene / 1 h / 60 °C
2: 5.3 g / triethylamine / CH2Cl2 / Ambient temperature
3: 1.) lithium diisopropylamide / 1.) THF, hexane, -70 deg C, 1 h, 2.) -60 deg C, 1 h
4: 50 percent / 2 M H2SO4 / H2O / 80 °C
5: 1.) N-methylmorpholine, isobutyl chloroformate / 1.) CH2Cl2, -20 deg C - (-15 deg C), 15 min, 2.) -10 deg C -> 2 deg C, 30 min
6: 100 percent / ammonia / methanol / 0.17 h
With 4-methyl-morpholine; thionyl chloride; sulfuric acid; ammonia; triethylamine; N,N-dimethyl-formamide; lithium diisopropyl amide; isobutyl chloroformate; In methanol; dichloromethane; water; toluene;
DOI:10.3891/acta.chem.scand.43-0476
Guidance literature:
Multi-step reaction with 5 steps
1: 5.3 g / triethylamine / CH2Cl2 / Ambient temperature
2: 1.) lithium diisopropylamide / 1.) THF, hexane, -70 deg C, 1 h, 2.) -60 deg C, 1 h
3: 50 percent / 2 M H2SO4 / H2O / 80 °C
4: 1.) N-methylmorpholine, isobutyl chloroformate / 1.) CH2Cl2, -20 deg C - (-15 deg C), 15 min, 2.) -10 deg C -> 2 deg C, 30 min
5: 100 percent / ammonia / methanol / 0.17 h
With 4-methyl-morpholine; sulfuric acid; ammonia; triethylamine; lithium diisopropyl amide; isobutyl chloroformate; In methanol; dichloromethane; water;
DOI:10.3891/acta.chem.scand.43-0476
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