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(1R,2S)-2-((S)-1-Amino-propyl)-1-phenyl-cyclopropanecarboxylic acid diethylamide

Base Information Edit
  • Chemical Name:(1R,2S)-2-((S)-1-Amino-propyl)-1-phenyl-cyclopropanecarboxylic acid diethylamide
  • CAS No.:172015-94-0
  • Molecular Formula:C17H26N2O
  • Molecular Weight:274.406
  • Hs Code.:
  • Mol file:172015-94-0.mol
(1R,2S)-2-((S)-1-Amino-propyl)-1-phenyl-cyclopropanecarboxylic acid diethylamide

Synonyms:(1R,2S)-2-((S)-1-Amino-propyl)-1-phenyl-cyclopropanecarboxylic acid diethylamide

Suppliers and Price of (1R,2S)-2-((S)-1-Amino-propyl)-1-phenyl-cyclopropanecarboxylic acid diethylamide
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Chemical Property of (1R,2S)-2-((S)-1-Amino-propyl)-1-phenyl-cyclopropanecarboxylic acid diethylamide Edit
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Technology Process of (1R,2S)-2-((S)-1-Amino-propyl)-1-phenyl-cyclopropanecarboxylic acid diethylamide

There total 10 articles about (1R,2S)-2-((S)-1-Amino-propyl)-1-phenyl-cyclopropanecarboxylic acid diethylamide 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: 1.) NaNH2 / 1) benzene, rt, 3 h; 2) benzene, rt, 2 h
2: aq. KOH / ethanol / 15 h / Heating
3: 1.) BuLi / 1) THF, hexane, 0 - -78 deg C; 2) THF, hexane, -78 deg C, 2 h
4: 1.) oxalyl chloride, DMSO, 2.) Et3N / 1) CH2Cl2, -78 deg C, 2 h; 2) CH2Cl2, -78 deg C, 1 h
5: tetrahydrofuran / 2 h / -20 °C
6: PDC, molecular sieves 4 Angstroem / CH2Cl2 / 2 h / Ambient temperature
7: DIBAL-H / tetrahydrofuran; hexane / 1 h / -78 °C
8: NaN3, Ph3P, CBr4 / dimethylformamide / 3 h / Ambient temperature
9: H2 / Pd/C / methanol / 1.5 h / Ambient temperature
With potassium hydroxide; dipyridinium dichromate; n-butyllithium; sodium azide; oxalyl dichloride; carbon tetrabromide; 4 A molecular sieve; hydrogen; diisobutylaluminium hydride; sodium amide; dimethyl sulfoxide; triethylamine; triphenylphosphine; palladium on activated charcoal; In tetrahydrofuran; methanol; ethanol; hexane; dichloromethane; N,N-dimethyl-formamide;
DOI:10.1021/jo9518056
Guidance literature:
With hydrogen; palladium on activated charcoal; In methanol; for 1.5h; Ambient temperature;
DOI:10.1021/jo9518056
Guidance literature:
Multi-step reaction with 8 steps
1: aq. KOH / ethanol / 15 h / Heating
2: 1.) BuLi / 1) THF, hexane, 0 - -78 deg C; 2) THF, hexane, -78 deg C, 2 h
3: 1.) oxalyl chloride, DMSO, 2.) Et3N / 1) CH2Cl2, -78 deg C, 2 h; 2) CH2Cl2, -78 deg C, 1 h
4: tetrahydrofuran / 2 h / -20 °C
5: PDC, molecular sieves 4 Angstroem / CH2Cl2 / 2 h / Ambient temperature
6: DIBAL-H / tetrahydrofuran; hexane / 1 h / -78 °C
7: NaN3, Ph3P, CBr4 / dimethylformamide / 3 h / Ambient temperature
8: H2 / Pd/C / methanol / 1.5 h / Ambient temperature
With potassium hydroxide; dipyridinium dichromate; n-butyllithium; sodium azide; oxalyl dichloride; carbon tetrabromide; 4 A molecular sieve; hydrogen; diisobutylaluminium hydride; dimethyl sulfoxide; triethylamine; triphenylphosphine; palladium on activated charcoal; In tetrahydrofuran; methanol; ethanol; hexane; dichloromethane; N,N-dimethyl-formamide;
DOI:10.1021/jo9518056
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