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2-[(5-BROMO-2-THIENYL)CARBONYL]BENZENECARBOXYLIC ACID synthesis

2synthesis methods
14282-76-9 Synthesis
2-Bromo-3-methylthiophene

14282-76-9
314 suppliers
$7.00/5g

2-[(5-BROMO-2-THIENYL)CARBONYL]BENZENECARBOXYLIC ACID

205644-06-0
8 suppliers
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Yield:-

Reaction Conditions:

aluminium trichloride in 1,1-dichloroethane;

Steps:

42 Synthesis of (R)-1-(α-phenylethylamino)-4-(4-methyl-2-thienyl)phthalazine (Compound No. 189 in Table 1)

Example 42 Synthesis of (R)-1-(α-phenylethylamino)-4-(4-methyl-2-thienyl)phthalazine (Compound No. 189 in Table 1) 1.90 g of phthalic anhydride and 3.58 g of aluminum chloride were dissolved in 40 ml of dichloroethane, and 2-bromo-3-methylthiophene was added dropwise to the solution at room temperature. After stirring the solution for 4 hours, the reaction solution was poured into a 1-N hydrochloric acid under cooling with ice, and extracted with chloroform. By purifying the extract by silica gel chromatography (eluent: chloroform, ethyl acetate), 1.70 g of o-(5-bromo-2-thenoyl)benzoic acid was obtained.

References:

US5462941,1995,A