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2,3-Dibromo-4-oxo-but-2-enoic acid synthesis

3synthesis methods
2,3-Dibromo-4-oxo-but-2-enoic acid

90994-06-2
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1073-70-7 Synthesis
4-Chlorophenylhydrazine hydrochloride

1073-70-7
516 suppliers
$5.00/10g

14132-96-8 Synthesis
4,5-Dibromo-2-(4-chloro-phenyl)-2H-pyridazin-3-one

14132-96-8
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Yield:14132-96-8 71%

Reaction Conditions:

with hydrogenchloride in water; for 32 h;

Steps:

4.1.6 4-(4,5-Dibromo-6-oxopyridazin-1(6H)-yl)benzonitrile (46) (Scheme 1C)

General procedure: A suspension of 4-hydrazinylbenzonitrile hydrochloride (42) (9.360g, 55.19mmol, 1.25 equiv) in 6M HCl (220mL) was added to a solution/suspension of mucobromic acid (45) (11.430g, 44.32mmol, 1.00 equiv) in 6M HCl (300mL), and the resulting suspension was stirred at 65-95°C for 18h, when TLC analysis indicated the reaction was complete.28 The viscous canary yellow suspension was cooled to 20°C and the solid was collected by filtration and washed sequentially with water and hexanes. The dried crude product was triturated with MeOH to furnish 46 (10.047g, 64%) as an amorphous off-white solid.

References:

Brooke, Darby G.;Van Dam, Ellen M.;Watts, Colin K.W.;Khoury, Amanda;Dziadek, Marie A.;Brooks, Hilary;Graham, Lisa-Jane K.;Flanagan, Jack U.;Denny, William A. [Bioorganic and Medicinal Chemistry,2014,vol. 22,# 3,p. 1029 - 1039]