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18162-48-6872-50-4Methylene ChloridenaphthaleneTHFTitanium Dioxide
10371-50-3

2-Phenyl-3-methyl-1-benzothiophene synthesis

6synthesis methods
3-METHYLBENZO[B]THIOPHENE

1455-18-1
161 suppliers
$8.00/1g

108-86-1 Synthesis
Bromobenzene

108-86-1
513 suppliers
$10.00/5g

2-Phenyl-3-methyl-1-benzothiophene

10371-50-3
2 suppliers
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Yield:10371-50-3 85%

Reaction Conditions:

with potassium carbonate;Trimethylacetic acid in N,N-dimethyl acetamide at 120; for 20 h;Inert atmosphere;

References:

Ohno, Aya;Sato, Takuma;Mase, Toshiaki;Uozumi, Yasuhiro;Yamada, Yoichi M. A. [Advanced Synthesis and Catalysis,2020,vol. 362,# 21,p. 4687 - 4698] Location in patent:supporting information

3-METHYLBENZO[B]THIOPHENE

1455-18-1
161 suppliers
$8.00/1g

591-50-4 Synthesis
Iodobenzene

591-50-4
490 suppliers
$10.00/1g

2-Phenyl-3-methyl-1-benzothiophene

10371-50-3
2 suppliers
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References
673-32-5 Synthesis
1-PHENYL-1-PROPYNE

673-32-5
132 suppliers
$11.00/1g

1,3-Dihydro-2-benzothiophene-1,3-dione

5698-59-9
13 suppliers
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2-Phenyl-3-methyl-1-benzothiophene

10371-50-3
2 suppliers
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Benzo[b]thiophene, 2-methyl-3-phenyl-

57642-62-3
0 suppliers
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References
673-32-5 Synthesis
1-PHENYL-1-PROPYNE

673-32-5
132 suppliers
$11.00/1g

2-Bromothioanisole

19614-16-5
165 suppliers
$6.00/1g

2-Phenyl-3-methyl-1-benzothiophene

10371-50-3
2 suppliers
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Benzo[b]thiophene, 2-methyl-3-phenyl-

57642-62-3
0 suppliers
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References
673-32-5 Synthesis
1-PHENYL-1-PROPYNE

673-32-5
132 suppliers
$11.00/1g

2-IODOTHIOANISOLE

33775-94-9
102 suppliers
$16.00/250mg

2-Phenyl-3-methyl-1-benzothiophene

10371-50-3
2 suppliers
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References