(E)-3-(2-tert-Butylsulfanyl-phenyl)-2-cyano-N-(2-diethylamino-ethyl)-acrylamide

Base Information

Chemical Name:(E)-3-(2-tert-Butylsulfanyl-phenyl)-2-cyano-N-(2-diethylamino-ethyl)-acrylamide
CAS No.:117194-85-1
Molecular Formula:C₂₀H₂₉N₃OS
Molecular Weight:359.536
Hs Code.:

Synonyms:(E)-3-(2-tert-Butylsulfanyl-phenyl)-2-cyano-N-(2-diethylamino-ethyl)-acrylamide

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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 (E)-3-(2-tert-Butylsulfanyl-phenyl)-2-cyano-N-(2-diethylamino-ethyl)-acrylamide

Chemical Property:

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Technology Process of (E)-3-(2-tert-Butylsulfanyl-phenyl)-2-cyano-N-(2-diethylamino-ethyl)-acrylamide

There total 3 articles about (E)-3-(2-tert-Butylsulfanyl-phenyl)-2-cyano-N-(2-diethylamino-ethyl)-acrylamide 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%

: 15029-13-7
Cyanessigsaeure-β-diethylamino-ethylamid

: 65924-65-4
2-(tert-butylthio)benzaldehyde

: 117194-85-1
(E)-3-(2-tert-Butylsulfanyl-phenyl)-2-cyano-N-(2-diethylamino-ethyl)-acrylamide

: 115-11-7,15220-85-6
isobutene

Guidance literature:: With piperidine; In benzene; for 60h; Heating;

Reference yield:

: 100-36-7
N,N-diethylethylenediamine

: 117194-85-1
(E)-3-(2-tert-Butylsulfanyl-phenyl)-2-cyano-N-(2-diethylamino-ethyl)-acrylamide

Guidance literature:: Multi-step reaction with 2 steps

1: 90 percent / 24 h / 40 °C

2: 85 percent / piperidine / benzene / 60 h / Heating

With piperidine; In benzene;

Reference yield:

: 552-89-6
2-nitro-benzaldehyde

: 117194-85-1
(E)-3-(2-tert-Butylsulfanyl-phenyl)-2-cyano-N-(2-diethylamino-ethyl)-acrylamide

Guidance literature:: Multi-step reaction with 2 steps

1: 87 percent / K₂CO₃ / dimethylformamide / 30 h, 100 deg C, then 12 h, room temperature

2: 85 percent / piperidine / benzene / 60 h / Heating

With piperidine; potassium carbonate; In N,N-dimethyl-formamide; benzene;