5'-BROMO-2'-HYDROXY-3'-NITROACETOPHENONE
5'-BROMO-2'-HYDROXY-3'-NITROACETOPHENONE Basic information
- Product Name:
- 5'-BROMO-2'-HYDROXY-3'-NITROACETOPHENONE
- Synonyms:
-
- 1-(5-BROMO-2-HYDROXY-3-NITROPHENYL)ETHANONE
- 3-BROMO-6-HYDROXY-5-NITRO ACETOPHENONE
- 5-BROMO-2-HYDROXY-3-NITROACETOPHENONE
- JRH-01018, 1-(5-Bromo-2-hydroxy-3-nitrophenyl)ethanone, 97%
- 5'-Bromo-2'-hydroxy-3'-nitroacetophenone >
- Ethanone, 1-(5-bromo-2-hydroxy-3-nitrophenyl)-
- 1-(5-Bromo-2-hydroxy-3-nitrophenyl)ethan-1-one
- 5'-Bromo-2'-hydroxy-3'-nitroacetophenone
- CAS:
- 70978-54-0
- MF:
- C8H6BrNO4
- MW:
- 260.04
- Product Categories:
-
- Aromatic Acetophenones & Derivatives (substituted)
- Building Blocks
- C7 to C8
- Carbonyl Compounds
- Chemical Synthesis
- Ketones
- Organic Building Blocks
- Mol File:
- 70978-54-0.mol
5'-BROMO-2'-HYDROXY-3'-NITROACETOPHENONE Chemical Properties
- Melting point:
- 129-132 °C(lit.)
- Boiling point:
- 272.9℃
- Density
- 1.763
- Flash point:
- 118.9℃
- storage temp.
- Sealed in dry,Room Temperature
- form
- powder to crystal
- pka
- 6.47±0.38(Predicted)
- color
- Light yellow to Yellow to Orange
- CAS DataBase Reference
- 70978-54-0(CAS DataBase Reference)
MSDS
- Language:English Provider:SigmaAldrich
5'-BROMO-2'-HYDROXY-3'-NITROACETOPHENONE Usage And Synthesis
Uses
5'-Bromo-2'-hydroxy-3'-nitroacetophenone is used as a chemical reagent in the synthesis of amides and benzoxazoles directly using a sulfate catalyst and microwaves. 1-(5-Bromo-2-hydroxy-3-nitrophen yl)ethanone is used in studies involving HIV-1 integrase inhibitors.
Preparation
Preparation by nitration of 5-bromo-2-hydroxyacetophenone in refluxing carbon tetrachloride (88%).
Synthesis
1450-75-5
70978-54-0
1. Synthesis of 5-bromo-2-hydroxy-3-nitroacetophenone To a solution of 5-bromo-2-hydroxyacetophenone (23.7 g, 0.110 mol) in carbon tetrachloride (90 mL) was slowly added concentrated nitric acid (17.2 mL). The reaction mixture was stirred at 75 °C for 50 min and subsequently cooled to room temperature. The precipitated solid was collected by filtration and washed with cold carbon tetrachloride. After vacuum drying, 20.9 g of the target product 5-bromo-2-hydroxy-3-nitroacetophenone was obtained as a light yellow solid in 73% yield. 1H NMR (300 MHz, CDCl3) δ: 2.73 (s, 3H), 8.14 (d, 1H), 8.31 (d, 1H), 12.92 (s, 1H).
References
[1] Patent: US5990142, 1999, A
[2] Patent: EP1391451, 2004, A1. Location in patent: Page 113
[3] Patent: WO2017/221002, 2017, A1. Location in patent: Page/Page column 92
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5'-BROMO-2'-HYDROXY-3'-NITROACETOPHENONE(70978-54-0)Related Product Information
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