(3-bromo-4,5-dichloro-1H-pyrrol-2-yl)(2,3,4-trimethoxyphenyl)methanone

Base Information

Chemical Name:(3-bromo-4,5-dichloro-1H-pyrrol-2-yl)(2,3,4-trimethoxyphenyl)methanone
CAS No.:1448592-55-9
Molecular Formula:C₁₄H₁₂BrCl₂NO₄
Molecular Weight:409.064
Hs Code.:

Synonyms:(3-bromo-4,5-dichloro-1H-pyrrol-2-yl)(2,3,4-trimethoxyphenyl)methanone

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Chemical Property of (3-bromo-4,5-dichloro-1H-pyrrol-2-yl)(2,3,4-trimethoxyphenyl)methanone

Chemical Property:

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Technology Process of (3-bromo-4,5-dichloro-1H-pyrrol-2-yl)(2,3,4-trimethoxyphenyl)methanone

There total 4 articles about (3-bromo-4,5-dichloro-1H-pyrrol-2-yl)(2,3,4-trimethoxyphenyl)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:

: 1448592-66-2
3-bromo-4,5-dichloro-1H-pyrrole-2-carboxylic acid methoxymethyl amide

: 114605-54-8
2,3,4-trimethoxyphenylmagnesium bromide

: 1448592-55-9
(3-bromo-4,5-dichloro-1H-pyrrol-2-yl)(2,3,4-trimethoxyphenyl)methanone

Guidance literature:: In tetrahydrofuran; at 0 ℃; for 1h;

Reference yield:

: 368211-06-7
1H-pyrrole-2-carboxylic acid methoxymethylamide

: 1448592-55-9
(3-bromo-4,5-dichloro-1H-pyrrol-2-yl)(2,3,4-trimethoxyphenyl)methanone

Guidance literature:: Multi-step reaction with 3 steps

1: sulfuryl dichloride / dichloromethane / 0 °C

2: N-Bromosuccinimide / 1,2-dichloro-ethane / 3 h / 90 °C

3: tetrahydrofuran / 1 h / 0 °C

With N-Bromosuccinimide; sulfuryl dichloride; In tetrahydrofuran; dichloromethane; 1,2-dichloro-ethane;

Reference yield:

: 2199-43-1
ethyl 1H-pyrrole-2-carboxylate

: 1448592-55-9
(3-bromo-4,5-dichloro-1H-pyrrol-2-yl)(2,3,4-trimethoxyphenyl)methanone

Guidance literature:: Multi-step reaction with 4 steps

1: lithium hexamethyldisilazane / tetrahydrofuran / 1 h / -78 °C

2: sulfuryl dichloride / dichloromethane / 0 °C

3: N-Bromosuccinimide / 1,2-dichloro-ethane / 3 h / 90 °C

4: tetrahydrofuran / 1 h / 0 °C

With N-Bromosuccinimide; sulfuryl dichloride; lithium hexamethyldisilazane; In tetrahydrofuran; dichloromethane; 1,2-dichloro-ethane;