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ChemicalBook CAS DataBase List 2-BroMo-5,7-dihydro-7,7-diMethyl-5-phenyl-indeno[2,1-b]carbazole

2-BroMo-5,7-dihydro-7,7-diMethyl-5-phenyl-indeno[2,1-b]carbazole synthesis

9synthesis methods

The resulting 12,12-dimethyl-10-phenyl-10,12-dihydroindeno[2,1-b]carbazole (7.5 g) and DMF (53 ml) were added to a reaction vessel. N-bromosuccinimide (3.72 g) was added under ice-cooled conditions, and the mixture was stirred for 9 hours and then left for one night. Water (260 ml) was added, and the mixture was subjected to filtration to obtain a brownish white powder of 7-bromo-12,12-dimethyl-10-phenyl-10,12-dihydroindeno[2,1-b]carbazole (8.67 g; yield 94.6%).
1257220-43-1 Synthesis
5,7-dihydro-7,7-diMethyl-5-phenyl-indeno[2,1-b]carbazole

1257220-43-1
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2-BroMo-5,7-dihydro-7,7-diMethyl-5-phenyl-indeno[2,1-b]carbazole

1257220-44-2
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Yield: 94.6%

Reaction Conditions:

with N-Bromosuccinimide in N,N-dimethyl-formamide

Steps:

1
The resulting 12,12-dimethyl-10-phenyl-10,12-dihydroindeno[2,1-b]carbazole (7.5 g) and DMF (53 ml) were added to a reaction vessel. N-bromosuccinimide (3.72 g) was added under ice-cooled conditions, and the mixture was stirred for 9 hours and then left for one night. Water (260 ml) was added, and the mixture was subjected to filtration to obtain a brownish white powder of 7-bromo-12,12-dimethyl-10-phenyl-10,12-dihydroindeno[2,1-b]carbazole (8.67 g; yield 94.6%).

References:

Hodogaya Chemical Co., Ltd.;YOKOYAMA, Norimasa;NAGAOKA, Makoto;TOGASHI, Kazunori;KASE, Kouki;TAKAHASHI, Eiji EP2599773, 2013, A1 Location in patent:Paragraph 0195

1257220-43-1 Synthesis
5,7-dihydro-7,7-diMethyl-5-phenyl-indeno[2,1-b]carbazole

1257220-43-1
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2-BroMo-5,7-dihydro-7,7-diMethyl-5-phenyl-indeno[2,1-b]carbazole

1257220-44-2
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inquiry

1257220-47-5 Synthesis
5,7-Dihydro-7,7-dimethyl-indeno[2,1-b]carbazole

1257220-47-5
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$23.00/250mg

2-BroMo-5,7-dihydro-7,7-diMethyl-5-phenyl-indeno[2,1-b]carbazole

1257220-44-2
46 suppliers
inquiry