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Quinoline, 2-(3-bromophenyl)- synthesis

9synthesis methods
5344-90-1 Synthesis
2-Aminobenzyl alcohol

5344-90-1
323 suppliers
$6.00/5g

2142-63-4 Synthesis
3'-Bromoacetophenone

2142-63-4
390 suppliers
$5.00/10g

Quinoline, 2-(3-bromophenyl)-

108062-54-0
1 suppliers
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Yield:108062-54-0 85%

Reaction Conditions:

with [(p-cymene)Ru(BiBzImH2)Cl][Cl];caesium carbonate in tert-Amyl alcohol at 125; for 12 h;

Steps:

4.4. Procedure for acceptorless dehydrogenative coupling of ketoneswith o-aminobenzyl alcohols to quinolines catalyzed by [(p-cymene)Ru(BiBzImH2)Cl][Cl]

General procedure: In a round-bottomed flask with a condenser tube were added oaminobenzylalcohols 1 (1 mmol) and ketones 2 (1.2 mmol, 1.2equiv), cat. 1 (6 mg, 0.01 mmol, 1 mol %), Cs2CO3 (163 mg,0.5 mmol, 0.5 equiv) and tert-amyl alcohol (1 mL). The reactionmixture was heated at 125 C in an oil bath for 12 h and thencooled to ambient temperature, concentrated in vacuo and purifiedby flash column chromatography with hexane/ethyl acetate (10:1,v/v) to afford corresponding products.

References:

Xu, Xiangchao;Ai, Yao;Wang, Rongzhou;Liu, Liping;Yang, Jiazhi;Li, Feng [Journal of Catalysis,2021,vol. 395,p. 340 - 349]

5344-90-1 Synthesis
2-Aminobenzyl alcohol

5344-90-1
323 suppliers
$6.00/5g

52780-14-0 Synthesis
3-BROMO-ALPHA-METHYLBENZYL ALCOHOL

52780-14-0
92 suppliers
$10.00/1g

Quinoline, 2-(3-bromophenyl)-

108062-54-0
1 suppliers
inquiry