N-{3-[(allylmethylamino)methyl]-5-nitrophenyl}-2,2,2-trifluoroacetamide

Base Information

Chemical Name:N-{3-[(allylmethylamino)methyl]-5-nitrophenyl}-2,2,2-trifluoroacetamide
CAS No.:1354567-04-6
Molecular Formula:C₁₃H₁₄F₃N₃O₃
Molecular Weight:317.268
Hs Code.:

Synonyms:N-{3-[(allylmethylamino)methyl]-5-nitrophenyl}-2,2,2-trifluoroacetamide

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Chemical Property of N-{3-[(allylmethylamino)methyl]-5-nitrophenyl}-2,2,2-trifluoroacetamide

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Technology Process of N-{3-[(allylmethylamino)methyl]-5-nitrophenyl}-2,2,2-trifluoroacetamide

There total 3 articles about N-{3-[(allylmethylamino)methyl]-5-nitrophenyl}-2,2,2-trifluoroacetamide 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: 96.0%

: 627-37-2
N-methyl-N-allylamine

: 1354566-92-9
2,2,2-trifluoro-N-(3-formyl-5-nitrophenyl)acetamide

: 1354567-04-6
N-{3-[(allylmethylamino)methyl]-5-nitrophenyl}-2,2,2-trifluoroacetamide

Guidance literature:: With sodium tris(acetoxy)borohydride; In dichloromethane; at 20 ℃;
DOI:10.1021/jm201112g

Reference yield:

: 1354566-85-0
3-nitro-5-(2,2,2-trifluoroacetylamino)benzoic acid methyl ester

: 1354567-04-6
N-{3-[(allylmethylamino)methyl]-5-nitrophenyl}-2,2,2-trifluoroacetamide

Guidance literature:: Multi-step reaction with 2 steps

1: diisobutylaluminium hydride / dichloromethane / 1 h / Cooling

2: sodium tris(acetoxy)borohydride / dichloromethane / 20 °C

With sodium tris(acetoxy)borohydride; diisobutylaluminium hydride; In dichloromethane;
DOI:10.1021/jm201112g

Reference yield:

: 23218-93-1
3-amino-5-nitro-benzoic acid methyl ester

: 1354567-04-6
N-{3-[(allylmethylamino)methyl]-5-nitrophenyl}-2,2,2-trifluoroacetamide

Guidance literature:: Multi-step reaction with 3 steps

1: triethylamine / tetrahydrofuran / 20 °C

2: diisobutylaluminium hydride / dichloromethane / 1 h / Cooling

3: sodium tris(acetoxy)borohydride / dichloromethane / 20 °C

With sodium tris(acetoxy)borohydride; diisobutylaluminium hydride; triethylamine; In tetrahydrofuran; dichloromethane;
DOI:10.1021/jm201112g