3-Fluoro-5-bromobenzyl bromide
3-Fluoro-5-bromobenzyl bromide Basic information
- Product Name:
- 3-Fluoro-5-bromobenzyl bromide
- Synonyms:
-
- 3-Fluoro-5-bromobenzyl bromide
- 1-Bromo-3-(bromomethyl)-5-fluorobenzene
- 5-bromo-3-fluorobenzyl bromide
- 1-Bromo-3-(bromomethyl)-5-fluorobenzene, alpha,3-Dibromo-5-fluorotoluene
- 3-Fluoro-5-bromoben bromide
- 3-Fluoro-5-broMobenl broMide
- 3-Fluoride-5-Bromine Bromine Benzyl
- Benzene, 1-bromo-3-(bromomethyl)-5-fluoro-
- CAS:
- 216755-57-6
- MF:
- C7H5Br2F
- MW:
- 267.92
- Product Categories:
-
- alkyl bromide| alkyl Fluorine
- Fluorine series
- Mol File:
- 216755-57-6.mol
3-Fluoro-5-bromobenzyl bromide Chemical Properties
- Melting point:
- 47 °C
- Boiling point:
- 251℃
- Density
- 1.923
- Flash point:
- 106℃
- storage temp.
- under inert gas (nitrogen or Argon) at 2–8 °C
- solubility
- soluble in Methanol
- form
- powder to crystal
- color
- White to Almost white
- Water Solubility
- Slightly soluble in water (2.9 g/L) (25°C).
- Sensitive
- Lachrymatory
3-Fluoro-5-bromobenzyl bromide Usage And Synthesis
Uses
3-Bromo-5-fluorobenzyl bromide is employed as a intermediate for pharmaceutical and chemical research.
Synthesis
216755-56-5
216755-57-6
General procedure for the synthesis of 3-fluoro-5-bromobenzyl bromide from (3-bromo-5-fluorophenyl)methanol: 3-bromo-5-fluorobenzyl alcohol (1.79 g, 8.39 mmol) and triphenylphosphine (3.65 g, 10.10 mmol) were dissolved in dichloromethane (45 mL), followed by addition of carbon tetrabromide (3.34 g, 10.10 mmol). The reaction mixture was stirred at room temperature overnight. After completion of the reaction, the solvent was removed by vacuum evaporation. The residue was treated with diethyl ether (50 mL) and stirred at room temperature to form a white slurry. The slurry was filtered through CeliteTM and the residue was washed with diethyl ether (2 x 50 mL). The filtrate and washings were combined and the crude product was obtained by vacuum evaporation. The crude product was purified by silica gel column chromatography using 2% ethyl acetate/hexane as eluent to afford 3-bromo-5-fluorobenzyl bromide (2.21 g, 98%). The structure of the product was confirmed by 1H NMR, 19F NMR and 13C NMR.1H NMR (400 MHz, CDCl3): δ 7.33 (s, 1H), 7.18 (ddd, JHF 8.2 Hz, JHH = 2.0,2.0 Hz, 1H), 7.05 (ddd, JHF = 9.0 Hz, JHH = 1.8,1.6 Hz. 1H), 4.38 (s, 2H); 19F NMR (377 MHz, CDCl3): δ -110.19 to -110.14 (m, 1F); 13C NMR (101 MHz, CDCl3): δ 162.67 (d, JCF = 252.1 Hz), 141.61 (d, JCF = 8.5 Hz), 128.17 ( d, JCF = 3.1 Hz), 122.94 (d, JCF = 10.0 Hz), 119.39 (d, JCF = 24.6 Hz), 115.34 (d, JCF = 22.3 Hz), 31.31 (d, JCF = 2.3 Hz).
References
[1] Patent: WO2016/54728, 2016, A1. Location in patent: Paragraph 00128
[2] Patent: WO2016/74068, 2016, A1. Location in patent: Paragraph 00122
[3] Patent: CN104447730, 2017, B. Location in patent: Paragraph 0149-0150
[4] Patent: US2007/249607, 2007, A1. Location in patent: Page/Page column 81
[5] Patent: US2002/49204, 2002, A1
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3-Fluoro-5-bromobenzyl bromide(216755-57-6)Related Product Information
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