N-Benzyl-2,2,2-trifluoro-N-((2R,3S)-2-hydroxy-3-p-tolylsulfanyl-2-trifluoromethyl-butyl)-acetamide

Base Information

• Chemical Name: N-Benzyl-2,2,2-trifluoro-N-((2R,3S)-2-hydroxy-3-p-tolylsulfanyl-2-trifluoromethyl-butyl)-acetamide
• CAS No.: 215114-59-3
• Molecular Formula: C₂₁H₂₁F₆NO₂S
• Molecular Weight: 465.46
• Mol file: 215114-59-3.mol

Synonyms:N-Benzyl-2,2,2-trifluoro-N-((2R,3S)-2-hydroxy-3-p-tolylsulfanyl-2-trifluoromethyl-butyl)-acetamide

Chemical Property of N-Benzyl-2,2,2-trifluoro-N-((2R,3S)-2-hydroxy-3-p-tolylsulfanyl-2-trifluoromethyl-butyl)-acetamide

Chemical Property:

Purity/Quality:

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

Useful:

Technology Process of N-Benzyl-2,2,2-trifluoro-N-((2R,3S)-2-hydroxy-3-p-tolylsulfanyl-2-trifluoromethyl-butyl)-acetamide

There total 4 articles about N-Benzyl-2,2,2-trifluoro-N-((2R,3S)-2-hydroxy-3-p-tolylsulfanyl-2-trifluoromethyl-butyl)-acetamide 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: 98.0%

trifluoroacetic anhydride (407-25-0) + (2R,3S)-2-(Benzylamino-methyl)-1,1,1-trifluoro-3-((R)-toluene-4-sulfinyl)-butan-2-ol (215114-47-9) → N-Benzyl-2,2,2-trifluoro-N-((2R,3S)-2-hydroxy-3-p-tolylsulfanyl-2-trifluoromethyl-butyl)-acetamide (215114-59-3)

Guidance literature:

With sodium iodide; In acetone; at -20 ℃; for 0.333333h;

DOI:10.1016/S0040-4020(98)83043-3

Reference yield:

(+)-(R)-ethyl p-tolyl sulfoxide (1519-40-0) → N-Benzyl-2,2,2-trifluoro-N-((2R,3S)-2-hydroxy-3-p-tolylsulfanyl-2-trifluoromethyl-butyl)-acetamide (215114-59-3)

Guidance literature:

Multi-step reaction with 3 steps

2: 90 percent / tetrahydrofuran / 24 h / Ambient temperature

3: 98 percent / NaI / acetone / 0.33 h / -20 °C

With sodium iodide; In tetrahydrofuran; acetone;

DOI:10.1016/S0040-4020(98)83043-3

Reference yield:

benzylamine (100-46-9) → N-Benzyl-2,2,2-trifluoro-N-((2R,3S)-2-hydroxy-3-p-tolylsulfanyl-2-trifluoromethyl-butyl)-acetamide (215114-59-3)

Guidance literature:

Multi-step reaction with 2 steps

1: 90 percent / tetrahydrofuran / 24 h / Ambient temperature

2: 98 percent / NaI / acetone / 0.33 h / -20 °C

With sodium iodide; In tetrahydrofuran; acetone;

DOI:10.1016/S0040-4020(98)83043-3

upstream raw materials:

trifluoroacetic anhydride

(2R,3S)-2-(Benzylamino-methyl)-1,1,1-trifluoro-3-((R)-toluene-4-sulfinyl)-butan-2-ol

(+)-(R)-ethyl p-tolyl sulfoxide

benzylamine

Downstream raw materials:

(S)-1-(N-benzyl-N-trifluoroacetyl)amino-2-trifluoromethylbutan-2-ol