N-((1R,2R,4S)-bicyclo[2.2.1]heptan-2-yl)-4-(trifluoromethyl)benzamide

Base Information

• Chemical Name: N-((1R,2R,4S)-bicyclo[2.2.1]heptan-2-yl)-4-(trifluoromethyl)benzamide
• CAS No.: 1389327-48-3
• Molecular Formula: C₁₅H₁₆F₃NO
• Molecular Weight: 283.293
• Mol file: 1389327-48-3.mol

Synonyms:N-((1R,2R,4S)-bicyclo[2.2.1]heptan-2-yl)-4-(trifluoromethyl)benzamide

Chemical Property of N-((1R,2R,4S)-bicyclo[2.2.1]heptan-2-yl)-4-(trifluoromethyl)benzamide

Chemical Property:

Purity/Quality:

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

Useful:

Technology Process of N-((1R,2R,4S)-bicyclo[2.2.1]heptan-2-yl)-4-(trifluoromethyl)benzamide

There total 1 articles about N-((1R,2R,4S)-bicyclo[2.2.1]heptan-2-yl)-4-(trifluoromethyl)benzamide 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:

Reference yield: 85.0%

norbornene (498-66-8) + p-trifluoromethylbenzamide (1891-90-3) → N-((1R,2R,4S)-bicyclo[2.2.1]heptan-2-yl)-4-(trifluoromethyl)benzamide (1389327-48-3)

Guidance literature:

p-trifluoromethylbenzamide; With (S)-(+)-5,5’-bis[di(3,5-di-tert-butyl-4-methoxyphenyl)phosphino]-4,4’-bi-1,3-benzodioxole; [IrCl(cyclooctene)₂]₂; In toluene; at 50 ℃; for 0.5h; Inert atmosphere;

norbornene; In toluene; at 120 ℃; for 24h; optical yield given as %ee; enantioselective reaction; Inert atmosphere;

DOI:10.1021/ja3052848

Reference yield: 87.0%

N-((1R,2R,4S)-bicyclo[2.2.1]heptan-2-yl)-4-(trifluoromethyl)benzamide (1389327-48-3) → (1R,2R,4S)-bicyclo[2.2.1]hept-2-ylamine (822-98-0,7242-92-4,31002-73-0,84235-33-6,84235-34-7,111137-34-9,121055-07-0,126752-99-6,130463-97-7)

Guidance literature:

With hydrogenchloride; at 120 ℃; for 72h; optical yield given as %ee; Inert atmosphere;

DOI:10.1021/ja3052848

upstream raw materials:

norbornene

p-trifluoromethylbenzamide

Downstream raw materials:

(1R,2R,4S)-bicyclo[2.2.1]hept-2-ylamine