(S)-N-[3,5-(bistrifluoromethyl)benzenesulfonyl]-N'-(2',2',2'-trifluoroethyl)-2-isopropylethylene diamine

Base Information

Chemical Name:(S)-N-[3,5-(bistrifluoromethyl)benzenesulfonyl]-N'-(2',2',2'-trifluoroethyl)-2-isopropylethylene diamine
CAS No.:652150-80-6
Molecular Formula:C₁₅H₁₇F₉N₂O₂S
Molecular Weight:460.364
Hs Code.:

Synonyms:(S)-N-[3,5-(bistrifluoromethyl)benzenesulfonyl]-N'-(2',2',2'-trifluoroethyl)-2-isopropylethylene diamine

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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 (S)-N-[3,5-(bistrifluoromethyl)benzenesulfonyl]-N'-(2',2',2'-trifluoroethyl)-2-isopropylethylene diamine

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Technology Process of (S)-N-[3,5-(bistrifluoromethyl)benzenesulfonyl]-N'-(2',2',2'-trifluoroethyl)-2-isopropylethylene diamine

There total 3 articles about (S)-N-[3,5-(bistrifluoromethyl)benzenesulfonyl]-N'-(2',2',2'-trifluoroethyl)-2-isopropylethylene diamine 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:

: 2026-48-4,473-75-6
(S)-valinol

: 652150-80-6
(S)-N-[3,5-(bistrifluoromethyl)benzenesulfonyl]-N'-(2',2',2'-trifluoroethyl)-2-isopropylethylene diamine

Guidance literature:: Multi-step reaction with 2 steps

1.1: DMAP; Et₃N / CH₂Cl₂ / -25 - 0 °C

1.2: 69 percent / MsCl / CH₂Cl₂ / 2 h / 0 °C

2.1: 12 h / 50 °C

With dmap; triethylamine; In dichloromethane;
DOI:10.1021/ja0391208

Reference yield:

: 39234-86-1
3,5-bis(trifluoromethyl)benzenesulfonyl chloride

: 652150-80-6
(S)-N-[3,5-(bistrifluoromethyl)benzenesulfonyl]-N'-(2',2',2'-trifluoroethyl)-2-isopropylethylene diamine

Guidance literature:: Multi-step reaction with 2 steps

1.1: DMAP; Et₃N / CH₂Cl₂ / -25 - 0 °C

1.2: 69 percent / MsCl / CH₂Cl₂ / 2 h / 0 °C

2.1: 12 h / 50 °C

With dmap; triethylamine; In dichloromethane;
DOI:10.1021/ja0391208