| Identification | More | [Name]
3-BROMO-5-FLUOROBENZALDEHYDE | [CAS]
188813-02-7 | [Synonyms]
3-BROMO-5-FLUOROBENZALDEHYDE
3-Bromo-5-fluorobenzaldehyde 98%
3-FLUORO-5-BROMOBENZALDEHYDE
3-Bromo-5-fluorobenzaldehyde98% | [Molecular Formula]
C7H4BrFO | [MDL Number]
MFCD04116319 | [Molecular Weight]
203.01 | [MOL File]
188813-02-7.mol |
| Chemical Properties | Back Directory | [Melting point ]
41-43℃ | [Boiling point ]
231.0±20.0 °C(Predicted) | [density ]
1.43 | [storage temp. ]
Inert atmosphere,2-8°C | [form ]
Solid | [Appearance]
White to yellow <41°C Solid,>43°C Liquid | [Water Solubility ]
Slightly soluble in water. | [Sensitive ]
Light Sensitive | [CAS DataBase Reference]
188813-02-7(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 . | [Hazard Note ]
Irritant | [HazardClass ]
IRRITANT | [HS Code ]
2913000090 |
| Hazard Information | Back Directory | [Uses]
3-Bromo-5-fluorobenzaldehyde is an intermediate in organic syntheses. Reatant in the synthesis of 3,4-diamino-3-cyclobutene-1,2-diones, 9,10-Dihydro-9,10-diboraanthracenes. | [Synthesis]
A 2M isopropylmagnesium chloride solution (10 mL, 20 mmol) was dissolved in 5 mL of tetrahydrofuran under ice bath conditions. To this solution was added a tetrahydrofuran solution of 1,3-dibromo-5-fluorobenzene (4.0 g, 15.70 mmol) and the reaction mixture was stirred for 2 hours. The reaction system was then warmed to 20°C and the reaction was continued for 30 minutes. After completion of the reaction, the system was cooled to 0°C, N,N-dimethylformamide (2.5 mL, 31.50 mmol) was slowly added dropwise and the reaction was stirred at this temperature for 1.5 hours. After that, the reaction mixture was stirred at room temperature for 12 hours. At the end of the reaction, the reaction was quenched by adding saturated ammonium chloride solution (20 mL). The reaction mixture was extracted with ethyl acetate (50 mL x 3), the organic phases were combined, dried over anhydrous sodium sulfate, filtered and the filtrate was concentrated under reduced pressure. Purification by silica gel column chromatography using eluent B afforded the target product 3-bromo-5-fluorobenzaldehyde (2.57 g, yellow liquid) in 81.0% yield. | [References]
[1] Patent: US6355648, 2002, B1. Location in patent: Page column 33-34
[2] Patent: CN103030646, 2016, B. Location in patent: Paragraph 0738; 0740-0743
[3] European Journal of Organic Chemistry, 2017, vol. 2017, # 4, p. 818 - 826
[4] Patent: US2007/88053, 2007, A1. Location in patent: Page/Page column 21
[5] Patent: CN105722823, 2016, A. Location in patent: Paragraph 0502; 0503 |
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