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4-Chloro-3-fluorobenzyl Bromide

Basic information Safety Supplier Related

4-Chloro-3-fluorobenzyl Bromide Basic information

Product Name:
4-Chloro-3-fluorobenzyl Bromide
Synonyms:
  • 4-Chloro-3-fluorobenzyl bromide 97%
  • 4-Chloro-3-fluorobenzylbromide97%
  • 4-(bromomethyl)-1-chloro-2-fluorobenzene
  • REF DUPL: 4-Chloro-3-fluorobenzyl bromide
  • alpha-Bromo-4-chloro-3-fluorotoluene 1-(Bromomethyl)-4-chloro-3-fluorobenzene
  • 4-(Bromomethyl)-1-chloro-2-fluorobenzene, alpha-Bromo-4-chloro-3-fluorotoluene
  • 4-Chloro-3-fluorobenzyl Bromide >
  • Benzene, 4-(bromomethyl)-1-chloro-2-fluoro-
CAS:
206362-80-3
MF:
C7H5BrClF
MW:
223.47
Mol File:
206362-80-3.mol
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4-Chloro-3-fluorobenzyl Bromide Chemical Properties

Melting point:
30-33℃
Boiling point:
227.1±25.0 °C(Predicted)
Density 
1.654±0.06 g/cm3(Predicted)
storage temp. 
Keep in dark place,Sealed in dry,Room Temperature
solubility 
soluble in Methanol
form 
powder to lump
color 
White to Light yellow to Light orange
Sensitive 
Lachrymatory
CAS DataBase Reference
206362-80-3(CAS DataBase Reference)
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Safety Information

Hazard Codes 
C
Risk Statements 
34
Safety Statements 
26-36/37/39-45
RIDADR 
3261
Hazard Note 
Corrosive/Lachrymatory
HazardClass 
CORROSIVE
HazardClass 
8
PackingGroup 
HS Code 
29039990
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4-Chloro-3-fluorobenzyl Bromide Usage And Synthesis

Chemical Properties

White solid

Synthesis

202925-10-8

206362-80-3

Step 1: Bromine (16.5 g, 0.103 mol) was added dropwise to a solution of triphenylphosphine (27.8 g, 0.103 mol) in dichloromethane (200 mL) at 0°C while stirring. After the dropwise addition was completed, stirring of the reaction mixture was continued for 10 minutes. Subsequently, 4-chloro-3-fluorobenzyl alcohol (15.8 g, 0.098 mol) was added and the reaction mixture was stirred for 30 minutes. Upon completion of the reaction, the reaction was quenched with ethanol and the mixture was poured into saturated sodium bicarbonate solution and extracted with dichloromethane. The organic phases were combined, dried with anhydrous sodium sulfate, filtered and concentrated. Purification by silica gel column chromatography afforded 4-(bromomethyl)-1-chloro-2-fluorobenzene (18.6 g, 85% yield).1H-NMR (400 MHz, CDCl3): δ = 7.27 (t, J = 7.9 Hz, 1H), 7.10 (dd, J = 7.9 Hz, 2.1 Hz, 1H), 7.04-6.99 (m, 1H). 4.32 (s, 2H).

References

[1] Patent: EP2952510, 2015, A1. Location in patent: Paragraph 0185

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