5-BROMOINDOLINE synthesis
- Product Name:5-BROMOINDOLINE
- CAS Number:22190-33-6
- Molecular formula:C8H8BrN
- Molecular Weight:198.06
22190-38-1
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22190-33-6
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Yield:22190-33-6 98.04%
Reaction Conditions:
with hydrogenchloride in ethanol;water at 78; for 4 h;Green chemistry;Solvent;Temperature;
Steps:
1.4 (4) Synthesis of 5-bromoindoline
A) A mixture of 38 g (0.16 mol) of N-acetyl-5-bromoindoline, 31 g of concentrated hydrochloric acid and 41 g of ethanol was charged into a reaction flask and stirred uniformly to obtain the reaction mixture I; B) reaction mixture I at 78 , reaction 4h, the chromatographic monitoring of raw materials disappeared; C) neutralized with 55 g of sodium hydroxide solution; D) to obtain organic phase J and water phase K; E) The organic phase J was extracted three times with 445 g of chloroform. The organic layers were combined and the solvent was recovered to give 30.74 g of 5-bromoindoline, yield 98.04% and content ≥99%.
References:
Sinosteel Anshan Research Institute of Thermo-energy Co., Ltd.;Wang, Shoukai;Wang, Haiyang;Zhao, Sujuan;Zhao, Wei;Ma, Saiyong;Xu, Haoran;Jin, Dan;Chen, Xing CN106432040, 2017, A Location in patent:Paragraph 0108-0113; 0135-0140; 0162-0167
10075-50-0
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22190-33-6
246 suppliers
$9.00/1g
496-15-1
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$8.00/10g
22190-33-6
246 suppliers
$9.00/1g
22190-38-1
129 suppliers
$40.10/1g
22190-33-6
246 suppliers
$9.00/1g
64-17-5
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918529-91-6
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22190-33-6
246 suppliers
$9.00/1g