Identification | More | [Name]
1-BROMO-3-ETHYLBENZENE | [CAS]
2725-82-8 | [Synonyms]
1-BROMO-3-ETHYLBENZENE 3-BROMOETHYL BENZENE 3-ethylbromobenzene | [Molecular Formula]
C8H9Br | [MDL Number]
MFCD00156128 | [Molecular Weight]
185.06 | [MOL File]
2725-82-8.mol |
Chemical Properties | Back Directory | [Appearance]
Clear colourless to light yellow liquid | [Melting point ]
-20.49°C (estimate) | [Boiling point ]
85 °C | [density ]
1,3493 g/cm3 | [refractive index ]
1.5465 | [Fp ]
76-78°C/10mm | [storage temp. ]
Sealed in dry,Room Temperature | [solubility ]
Chloroform (Slightly), Ethyl Acetate (Slightly), Methanol (Slightly) | [form ]
Oil | [color ]
Clear Colorless | [Detection Methods]
GC | [CAS DataBase Reference]
2725-82-8(CAS DataBase Reference) |
Safety Data | Back Directory | [Hazard Codes ]
Xi | [Risk Statements ]
R36/37/38:Irritating to eyes, respiratory system and skin . | [Safety Statements ]
S26:In case of contact with eyes, rinse immediately with plenty of water and seek medical advice . S36/37/39:Wear suitable protective clothing, gloves and eye/face protection . S37/39:Wear suitable gloves and eye/face protection . | [HS Code ]
2903998090 |
Hazard Information | Back Directory | [Chemical Properties]
Clear colourless to light yellow liquid | [Uses]
1-Bromo-3-ethylbenzene is a useful synthetic intermediate. 1-Bromo-3-ethylbenzene is also used as a reagent to synthesize novel benzo[1,4]diazepin-2-one derivatives, which act as Endothelin receptor agonists and can possibly be used to reduce arterial blood pressure in humans. | [Synthesis]
The general procedure for synthesizing 3-bromoethylbenzene from 3-ethylaniline is as follows:Reference Example 1 Synthesis of 1-bromo-3-ethylbenzene. To a 50% aqueous sulfuric acid solution (43.6 g) containing 3-ethylaniline (10.0 g, 82.5 mmol), an aqueous sodium nitrite solution (16.5 mL containing 6.83 g, 99.0 mmol) was slowly added dropwise at 0°C, and the dropwise process lasted for 30 minutes. The resulting reaction mixture was continued to be stirred at 0°C for 45 min. Subsequently, the prepared diazonium salt solution was added in batches to a 48% hydrobromic acid solution (82.5 mL) containing copper(I) bromide (12.4 g, 86.6 mmol) while maintaining a mild reflux condition. After addition, the reaction mixture was heated to reflux for 30 minutes. Upon completion of the reaction, the mixture was cooled to room temperature and extracted with ether. The extract was washed sequentially with 1N aqueous sodium hydroxide and saturated brine, dried over anhydrous sodium sulfate and concentrated under reduced pressure. The crude product obtained was purified by silica gel column chromatography (eluent: hexane/ethyl acetate=20:1) to give 3-bromoethylbenzene (6.13 g, 40% yield) as an oil.1H-NMR (CDCl3) δ: 1.23 (3H, t, J=7.5 Hz), 2.63 (2H, q, J=7.5 Hz), 7.11-7.20 (2H, m). 7.28-7.38 (2H, m). | [References]
[1] Patent: EP1354603, 2003, A1 [2] Patent: EP1402900, 2004, A1 [3] Patent: EP1402900, 2004, A1 [4] Patent: EP1364949, 2003, A1. Location in patent: Page/Page column 78 [5] Patent: EP1205478, 2002, A1 |
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