| Company Name: |
Alfa Aesar |
| Tel: |
400-6106006 |
| Email: |
saleschina@alfa-asia.com |
| Company Name: |
Energy Chemical |
| Tel: |
400-0056266 |
| Email: |
sales8178@energy-chemical.com |
|
| | 5'-Bromo-2'-hydroxy-3'-nitroacetophenone Basic information |
| | 5'-Bromo-2'-hydroxy-3'-nitroacetophenone Chemical Properties |
| Melting point | 129-132 °C(lit.) | | Boiling point | 272.9℃ | | density | 1.763 | | Fp | 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 | | InChI | 1S/C8H6BrNO4/c1-4(11)6-2-5(9)3-7(8(6)12)10(13)14/h2-3,12H,1H3 | | InChIKey | CLNIBJASCGZXHH-UHFFFAOYSA-N | | SMILES | CC(=O)c1cc(Br)cc(c1O)[N+]([O-])=O | | CAS DataBase Reference | 70978-54-0(CAS DataBase Reference) |
| Hazard Codes | Xi | | Risk Statements | 36/37/38 | | Safety Statements | 26-36 | | WGK Germany | 3 | | HS Code | 29145090 | | Storage Class | 11 - Combustible Solids | | Hazard Classifications | Eye Irrit. 2 Skin Irrit. 2 STOT SE 3 |
| | 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 | 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 |
| | 5'-Bromo-2'-hydroxy-3'-nitroacetophenone Preparation Products And Raw materials |
|