N-benzoyl-6,6,6-trifluoronorleucine ethyl ester

Base Information

Chemical Name:N-benzoyl-6,6,6-trifluoronorleucine ethyl ester
CAS No.:122489-89-8
Molecular Formula:C₁₅H₁₈F₃NO₃
Molecular Weight:317.308
Hs Code.:

Synonyms:N-benzoyl-6,6,6-trifluoronorleucine ethyl ester

Suppliers and Price of N-benzoyl-6,6,6-trifluoronorleucine ethyl ester

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Business phase:: The product has achieved commercial mass production^*data from LookChem market partment

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Chemical Property of N-benzoyl-6,6,6-trifluoronorleucine ethyl ester

Chemical Property:

Purity/Quality:

Safty Information:

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Hazard Codes:

MSDS Files:: SDS file from LookChem

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Technology Process of N-benzoyl-6,6,6-trifluoronorleucine ethyl ester

There total 3 articles about N-benzoyl-6,6,6-trifluoronorleucine ethyl ester 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: 100.0%

: 122489-86-5
ethyl (Z)-2-benzamido-5-(trifluoromethyl)-2-pentenoate

: 122489-89-8
N-benzoyl-6,6,6-trifluoronorleucine ethyl ester

Guidance literature:: With hydrogen; palladium on activated charcoal; In ethanol; for 2h; Ambient temperature;
DOI:10.1021/jo00280a014

Reference yield:

: 495-69-2,140480-84-8,21251-67-2,91787-63-2,66407-11-2
Hippuric Acid

: 122489-89-8
N-benzoyl-6,6,6-trifluoronorleucine ethyl ester

Guidance literature:: Multi-step reaction with 3 steps

1: 71 percent / lead(II) acetate trihydrate, acetic anhydride / tetrahydrofuran / 16 h / Heating

2: 57 percent / sodium / 2 h / Heating

3: 100 percent / H₂ / 10percent Pd/C / ethanol / 2 h / Ambient temperature

With hydrogen; sodium; lead acetate; acetic anhydride; palladium on activated charcoal; In tetrahydrofuran; ethanol;
DOI:10.1021/jo00280a014

Reference yield:

: 122519-46-4
2-phenyl-4-(4,4,4-trifluorobutylidene)-5-oxazolone

: 122489-89-8
N-benzoyl-6,6,6-trifluoronorleucine ethyl ester

Guidance literature:: Multi-step reaction with 2 steps

1: 57 percent / sodium / 2 h / Heating

2: 100 percent / H₂ / 10percent Pd/C / ethanol / 2 h / Ambient temperature

With hydrogen; sodium; palladium on activated charcoal; In ethanol;
DOI:10.1021/jo00280a014