N-[[2-bromo-4-[2-(3,5-dichlorophenyl)-2-(trifluoromethyl)-3H-thiophen-4-yl]phenyl]sulfanylmethyl]acetamide

Base Information

Chemical Name:N-[[2-bromo-4-[2-(3,5-dichlorophenyl)-2-(trifluoromethyl)-3H-thiophen-4-yl]phenyl]sulfanylmethyl]acetamide
CAS No.:1610615-91-2
Molecular Formula:C₂₀H₁₅BrCl₂F₃NOS₂
Molecular Weight:557.282
Hs Code.:

Synonyms:N-[[2-bromo-4-[2-(3,5-dichlorophenyl)-2-(trifluoromethyl)-3H-thiophen-4-yl]phenyl]sulfanylmethyl]acetamide

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Chemical Property of N-[[2-bromo-4-[2-(3,5-dichlorophenyl)-2-(trifluoromethyl)-3H-thiophen-4-yl]phenyl]sulfanylmethyl]acetamide

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Technology Process of N-[[2-bromo-4-[2-(3,5-dichlorophenyl)-2-(trifluoromethyl)-3H-thiophen-4-yl]phenyl]sulfanylmethyl]acetamide

There total 6 articles about N-[[2-bromo-4-[2-(3,5-dichlorophenyl)-2-(trifluoromethyl)-3H-thiophen-4-yl]phenyl]sulfanylmethyl]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:

: 1610609-39-6
4-(3-bromo-4-tert-butylsulfanyl-phenyl)-2-(3,5-dichlorophenyl)-2-(trifluoromethyl)-3H-thiophene

: 625-51-4
N-(hydroxymethyl)acetamide

: 1610615-91-2
N-[[2-bromo-4-[2-(3,5-dichlorophenyl)-2-(trifluoromethyl)-3H-thiophen-4-yl]phenyl]sulfanylmethyl]acetamide

Guidance literature:: With hydrogenchloride; In water; N,N-dimethyl-formamide; at 75 ℃; for 4h; Inert atmosphere;

Reference yield:

: 1610609-35-2
ethyl 3-(3-bromo-4-tert-butylsulfanyl-phenyl)-5-(3,5-dichlorophenyl)-3-hydroxy-5-(trifluoromethyl)tetrahydrothiophene-2-carboxylate

: 1610615-91-2
N-[[2-bromo-4-[2-(3,5-dichlorophenyl)-2-(trifluoromethyl)-3H-thiophen-4-yl]phenyl]sulfanylmethyl]acetamide

Guidance literature:: Multi-step reaction with 5 steps

1: lithium hydroxide; water / tetrahydrofuran / 20 °C

2: pyridine / 0 - 20 °C

3: N,N-dimethyl-formamide / 2 h / 100 °C

4: boron tribromide / dichloromethane / 2 h / 0 °C

5: hydrogenchloride / N,N-dimethyl-formamide; water / 4 h / 75 °C / Inert atmosphere

With pyridine; hydrogenchloride; water; boron tribromide; lithium hydroxide; In tetrahydrofuran; dichloromethane; water; N,N-dimethyl-formamide;

Reference yield:

: 1610609-40-9
(Z)-1-(3-bromo-4-tert-butylsulfanyl-phenyl)-3-(3,5-dichlorophenyl)-4,4,4-trifluoro-but-2-en-1-one

: 1610615-91-2
N-[[2-bromo-4-[2-(3,5-dichlorophenyl)-2-(trifluoromethyl)-3H-thiophen-4-yl]phenyl]sulfanylmethyl]acetamide

Guidance literature:: Multi-step reaction with 6 steps

1: triethylamine / tetrahydrofuran / 20 °C / Inert atmosphere

2: lithium hydroxide; water / tetrahydrofuran / 20 °C

3: pyridine / 0 - 20 °C

4: N,N-dimethyl-formamide / 2 h / 100 °C

5: boron tribromide / dichloromethane / 2 h / 0 °C

6: hydrogenchloride / N,N-dimethyl-formamide; water / 4 h / 75 °C / Inert atmosphere

With pyridine; hydrogenchloride; water; boron tribromide; triethylamine; lithium hydroxide; In tetrahydrofuran; dichloromethane; water; N,N-dimethyl-formamide;