(4-chlorophenyl)(2-(5-(hydroxymethyl)-3-methylisoxazol-4-yl)-4,5-dimethylthiophen-3-yl)methanone

Base Information

Chemical Name:(4-chlorophenyl)(2-(5-(hydroxymethyl)-3-methylisoxazol-4-yl)-4,5-dimethylthiophen-3-yl)methanone
CAS No.:1380089-51-9
Molecular Formula:C₁₈H₁₆ClNO₃S
Molecular Weight:361.849
Hs Code.:

Synonyms:(4-chlorophenyl)(2-(5-(hydroxymethyl)-3-methylisoxazol-4-yl)-4,5-dimethylthiophen-3-yl)methanone

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Chemical Property of (4-chlorophenyl)(2-(5-(hydroxymethyl)-3-methylisoxazol-4-yl)-4,5-dimethylthiophen-3-yl)methanone

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Technology Process of (4-chlorophenyl)(2-(5-(hydroxymethyl)-3-methylisoxazol-4-yl)-4,5-dimethylthiophen-3-yl)methanone

There total 5 articles about (4-chlorophenyl)(2-(5-(hydroxymethyl)-3-methylisoxazol-4-yl)-4,5-dimethylthiophen-3-yl)methanone 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:

: 14559-13-8
methyl 4,5-dimethylthiophene-3-carboxylate

: 1380089-51-9
(4-chlorophenyl)(2-(5-(hydroxymethyl)-3-methylisoxazol-4-yl)-4,5-dimethylthiophen-3-yl)methanone

Guidance literature:: Multi-step reaction with 4 steps

1: isopropylmagnesium bromide / tetrahydrofuran; cyclopentyl methyl ether / -20 - 0 °C

2: diethyl ether; tetrahydrofuran / 0.17 h / -40 °C

3: N-Bromosuccinimide / N,N-dimethyl-formamide / 2 h

4: potassium carbonate; water / (1,1'-bis(diphenylphosphino)ferrocene)palladium(II) dichloride / 5 h / 95 °C / Inert atmosphere

With N-Bromosuccinimide; water; isopropylmagnesium bromide; potassium carbonate; (1,1'-bis(diphenylphosphino)ferrocene)palladium(II) dichloride; In tetrahydrofuran; diethyl ether; cyclopentyl methyl ether; N,N-dimethyl-formamide;

Reference yield:

: 1380089-49-5
(4-chlorophenyl)(4,5-dimethylthiophen-3-yl)methanone

: 1380089-51-9
(4-chlorophenyl)(2-(5-(hydroxymethyl)-3-methylisoxazol-4-yl)-4,5-dimethylthiophen-3-yl)methanone

Guidance literature:: Multi-step reaction with 2 steps

1: N-Bromosuccinimide / N,N-dimethyl-formamide / 2 h

2: potassium carbonate; water / (1,1'-bis(diphenylphosphino)ferrocene)palladium(II) dichloride / 5 h / 95 °C / Inert atmosphere

With N-Bromosuccinimide; water; potassium carbonate; (1,1'-bis(diphenylphosphino)ferrocene)palladium(II) dichloride; In N,N-dimethyl-formamide;

Reference yield:

: 1380089-48-4
N-methoxy-N,4,5-trimethylthiophene-3-carboxamide

: 1380089-51-9
(4-chlorophenyl)(2-(5-(hydroxymethyl)-3-methylisoxazol-4-yl)-4,5-dimethylthiophen-3-yl)methanone

Guidance literature:: Multi-step reaction with 3 steps

1: diethyl ether; tetrahydrofuran / 0.17 h / -40 °C

2: N-Bromosuccinimide / N,N-dimethyl-formamide / 2 h

3: potassium carbonate; water / (1,1'-bis(diphenylphosphino)ferrocene)palladium(II) dichloride / 5 h / 95 °C / Inert atmosphere

With N-Bromosuccinimide; water; potassium carbonate; (1,1'-bis(diphenylphosphino)ferrocene)palladium(II) dichloride; In tetrahydrofuran; diethyl ether; N,N-dimethyl-formamide;