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2-Bromo-4,5-difluorobenzaldehyde

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2-Bromo-4,5-difluorobenzaldehyde Basic information
Product Name:2-Bromo-4,5-difluorobenzaldehyde
Synonyms:2-Bromo-4,5-difluorobenzaldehyde;Benzaldehyde, 2-bromo-4,5-difluoro-;2-Bromo-4,5-difluorobenzaldehyde,98%;2-Bromo-4,5-difluorobenzaldehyde ISO 9001:2015 REACH;5-difluorobenzaldehyde
CAS:476620-54-9
MF:C7H3BrF2O
MW:221
EINECS:
Product Categories:
Mol File:476620-54-9.mol
2-Bromo-4,5-difluorobenzaldehyde Structure
2-Bromo-4,5-difluorobenzaldehyde Chemical Properties
Boiling point 232.0±35.0 °C(Predicted)
density 1.758±0.06 g/cm3(Predicted)
storage temp. Inert atmosphere,2-8°C
form Powder
color Off-white
Water Solubility Slightly soluble in water.
Safety Information
HS Code 2913000090
MSDS Information
2-Bromo-4,5-difluorobenzaldehyde Usage And Synthesis
UsesIt is an important intermediate for pharmaceutical and organic synthesis.
Synthesis
(2-Bromo-4,5-difluorophenyl)methanol

476620-55-0

2-Bromo-4,5-difluorobenzaldehyde

476620-54-9

General procedure for the synthesis of 2-bromo-4,5-difluorobenzaldehyde from (2-bromo-4,5-difluorophenyl)methanol: (2-bromo-4,5-difluorophenyl)methanol (1.23 g, 5.50 mmol), triethylamine (1.39 g, 13.75 mmol) and dimethylsulfoxide (1.72 g, 22.00 mmol) were dissolved in dichloromethane (25 mL) in dichloromethane (25 mL) and cooled to 0°C. Subsequently, sulfur trioxide-pyridine complex (1.32 g, 8.25 mmol) was added in batches. The reaction mixture was stirred at 0 °C for 1 h. Triethylamine (1.39 g, 13.75 mmol), dimethyl sulfoxide (1.72 g, 22.00 mmol) and sulfur trioxide-pyridine complex (1.32 g, 8.25 mmol) were added again. After continued stirring at 0 °C for 30 min, the reaction solution was diluted with dichloromethane (50 mL) and washed sequentially with saturated sodium bicarbonate solution and saturated sodium thiosulfate solution. The organic phase was dried over anhydrous sodium sulfate, filtered and concentrated under reduced pressure. Purification by fast column chromatography (RediSep fast column, 230-400 mesh silica gel, eluent 10-30% ethyl acetate in hexane solution) afforded 2-bromo-4,5-difluorobenzaldehyde (0.47 g, 39% yield).1H NMR (300 MHz, CDCl3) δ 10.23 (s, 1H), 7.77 (m, 1H), 7.52 (m, 1H).

References[1] Patent: WO2010/55005, 2010, A1. Location in patent: Page/Page column 70-71
[2] Patent: WO2011/20193, 2011, A1. Location in patent: Page/Page column 18-19
[3] Patent: WO2011/57382, 2011, A1. Location in patent: Page/Page column 21
[4] Bioorganic and Medicinal Chemistry Letters, 2012, vol. 22, # 5, p. 1953 - 1957
2-Bromo-4,5-difluorobenzaldehyde Preparation Products And Raw materials
Raw materials(2-Bromo-4,5-difluorophenyl)methanol-->Triethylamine-->Dichloromethane-->Pyridine sulfur trioxide-->Dimethyl sulfoxide
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