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(R,R)-(+)-N-<(1phenyl)ethyl>-3-methyl-4,4,4-trichlorobutanamide

Base Information Edit
  • Chemical Name:(R,R)-(+)-N-<(1phenyl)ethyl>-3-methyl-4,4,4-trichlorobutanamide
  • CAS No.:93714-83-1
  • Molecular Formula:C13H16Cl3NO
  • Molecular Weight:308.635
  • Hs Code.:
  • Mol file:93714-83-1.mol
(R,R)-(+)-N-<(1phenyl)ethyl>-3-methyl-4,4,4-trichlorobutanamide

Synonyms:(R,R)-(+)-N-<(1phenyl)ethyl>-3-methyl-4,4,4-trichlorobutanamide

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Chemical Property of (R,R)-(+)-N-<(1phenyl)ethyl>-3-methyl-4,4,4-trichlorobutanamide Edit
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Technology Process of (R,R)-(+)-N-<(1phenyl)ethyl>-3-methyl-4,4,4-trichlorobutanamide

There total 10 articles about (R,R)-(+)-N-<(1phenyl)ethyl>-3-methyl-4,4,4-trichlorobutanamide 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 7 steps
1: 63 percent / pyridinium chlorochromate / CH2Cl2 / 3 h / Ambient temperature
2: 1.) tert-butylamine, CCl4; 2.) N-chlorosuccinimide
3: 76 percent / potassium permanganate / H2O / 0.33 h / 65 °C
4: 1.) Pb(OAc)4; 2.) LiCl / 1.) benzene; 2.) benzene, 80-85 deg C
5: 68 percent / 1.48 M DIBAL / toluene / 1 h
6: 85 percent / Jones reagent / acetone / 0.17 h
7: 1.) thionyl chloride / 1.) benzene, 1 h, reflux; 2.) benzene, ether, 20 min
With lead(IV) acetate; tetrachloromethane; potassium permanganate; N-chloro-succinimide; thionyl chloride; jones reagent; diisobutylaluminium hydride; tert-butylamine; pyridinium chlorochromate; lithium chloride; In dichloromethane; water; acetone; toluene;
DOI:10.1021/ja00287a036
Guidance literature:
Multi-step reaction with 2 steps
1: 85 percent / Jones reagent / acetone / 0.17 h
2: 1.) thionyl chloride / 1.) benzene, 1 h, reflux; 2.) benzene, ether, 20 min
With thionyl chloride; jones reagent; In acetone;
DOI:10.1021/ja00287a036
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