methyl 6-bromo-3-(bromomethyl)-7-[(1-methylethyl)oxy]-2-[3-(trifluoromethyl)phenyl]-4-quinolinecarboxylate

Base Information

Chemical Name:methyl 6-bromo-3-(bromomethyl)-7-[(1-methylethyl)oxy]-2-[3-(trifluoromethyl)phenyl]-4-quinolinecarboxylate
CAS No.:1336905-24-8
Molecular Formula:C₂₂H₁₈Br₂F₃NO₃
Molecular Weight:561.193
Hs Code.:

Synonyms:methyl 6-bromo-3-(bromomethyl)-7-[(1-methylethyl)oxy]-2-[3-(trifluoromethyl)phenyl]-4-quinolinecarboxylate

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Chemical Property of methyl 6-bromo-3-(bromomethyl)-7-[(1-methylethyl)oxy]-2-[3-(trifluoromethyl)phenyl]-4-quinolinecarboxylate

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Technology Process of methyl 6-bromo-3-(bromomethyl)-7-[(1-methylethyl)oxy]-2-[3-(trifluoromethyl)phenyl]-4-quinolinecarboxylate

There total 6 articles about methyl 6-bromo-3-(bromomethyl)-7-[(1-methylethyl)oxy]-2-[3-(trifluoromethyl)phenyl]-4-quinolinecarboxylate 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:

: 1336905-22-6
methyl 6-bromo-3-methyl-7-[(1-methylethyl)oxy]-2-[3-(trifluoromethyl)phenyl]-4-quinolinecarboxylate

: 1336905-24-8
methyl 6-bromo-3-(bromomethyl)-7-[(1-methylethyl)oxy]-2-[3-(trifluoromethyl)phenyl]-4-quinolinecarboxylate

Guidance literature:: With N-Bromosuccinimide; dibenzoyl peroxide; In tetrachloromethane; for 6h; Reflux;

Reference yield:

: 77337-82-7
1-bromo-2-methoxy-4-nitrobenzene

: 1336905-24-8
methyl 6-bromo-3-(bromomethyl)-7-[(1-methylethyl)oxy]-2-[3-(trifluoromethyl)phenyl]-4-quinolinecarboxylate

Guidance literature:: Multi-step reaction with 6 steps

1.1: hydrogen bromide / water / 20 h / Reflux

2.1: potassium carbonate / acetonitrile / 2 h / Reflux

3.1: nickel(II) chloride tetrahydrate / acetonitrile / 0.08 h / 0 °C

3.2: 0.08 h / 0 °C

4.1: ethanol / 1 h / Reflux

4.2: 19 h / 20 °C / Reflux

5.1: oxalyl dichloride / N,N-dimethyl-formamide / dichloromethane / 1 h

5.2: 1 h / 20 °C

6.1: dibenzoyl peroxide; N-Bromosuccinimide / tetrachloromethane / 6 h / Reflux

With N-Bromosuccinimide; oxalyl dichloride; hydrogen bromide; potassium carbonate; dibenzoyl peroxide; nickel(II) chloride tetrahydrate; N,N-dimethyl-formamide; In tetrachloromethane; ethanol; dichloromethane; water; acetonitrile;

Reference yield:

: 52427-05-1
2-bromo-5-nitrophenol

: 1336905-24-8
methyl 6-bromo-3-(bromomethyl)-7-[(1-methylethyl)oxy]-2-[3-(trifluoromethyl)phenyl]-4-quinolinecarboxylate

Guidance literature:: Multi-step reaction with 5 steps

1.1: potassium carbonate / acetonitrile / 2 h / Reflux

2.1: nickel(II) chloride tetrahydrate / acetonitrile / 0.08 h / 0 °C

2.2: 0.08 h / 0 °C

3.1: ethanol / 1 h / Reflux

3.2: 19 h / 20 °C / Reflux

4.1: oxalyl dichloride / N,N-dimethyl-formamide / dichloromethane / 1 h

4.2: 1 h / 20 °C

5.1: dibenzoyl peroxide; N-Bromosuccinimide / tetrachloromethane / 6 h / Reflux

With N-Bromosuccinimide; oxalyl dichloride; potassium carbonate; dibenzoyl peroxide; nickel(II) chloride tetrahydrate; N,N-dimethyl-formamide; In tetrachloromethane; ethanol; dichloromethane; acetonitrile;