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ChemicalBook CAS DataBase List 2,5-Di(4-formylphenyl)thiophene
193903-62-7

2,5-Di(4-formylphenyl)thiophene synthesis

4synthesis methods
3141-27-3 Synthesis
2,5-Dibromothiophene

3141-27-3
311 suppliers
$5.00/10g

87199-17-5 Synthesis
4-Formylphenylboronic acid

87199-17-5
432 suppliers
$8.00/5g

2,5-Di(4-formylphenyl)thiophene

193903-62-7
23 suppliers
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Yield:193903-62-7 86%

Reaction Conditions:

Stage #1: 2,5-dibromothiophen;4-formylphenylboronic acid,with potassium carbonate in N,N-dimethyl-formamide; for 0.5 h;Inert atmosphere;Suzuki Coupling;
Stage #2: with tetrakis(triphenylphosphine) palladium(0) in d7-N,N-dimethylformamide at 100; for 6 h;Inert atmosphere;Suzuki Coupling;

Steps:

1

(1)2,5-Bis(4-formylphenyl)thiophene BFT: First, 2,5-dibromothiophene (0.484 g, 2 mmol),4-formylphenylboronic acid (0.72 g, 4.8 mmol),K2CO3 (0.696g, 1N) and N,N-dimethylformamide (5mL) were mixed for 30 minutes under N2 atmosphere.Then put tetrakis(triphenylphosphine)palladium (0.115 g, 0.1 mmol),The reaction was stirred at 100 ° C for 6 hours.The reaction is completed,Natural cooling,The resulting orange suspension was filtered and extracted with chloroform.At last,Product column chromatography,The target product was a brown solid, 0.51 g.The yield was 86%.

References:

CN108484588,2018,A Location in patent:Paragraph 0043; 0044

126747-14-6 Synthesis
4-Cyanophenylboronic acid

126747-14-6
407 suppliers
$6.00/1g

2,5-Di(4-formylphenyl)thiophene

193903-62-7
23 suppliers
inquiry