ChemicalBook--->CAS DataBase List--->31928-44-6

31928-44-6

31928-44-6 Structure

31928-44-6 Structure
IdentificationBack Directory
[Name]

2-BROMO-4-CHLORO-1-IODOBENZENE
[CAS]

31928-44-6
[Synonyms]

2-BROMO-4-CHLORO-1-IODOBENZENE
1-Iodo-2-bromo-4-chlorobenzene
2-Bromo-1-iodo-4-chlorobenzene
[EINECS(EC#)]

1806241-263-5
[Molecular Formula]

C6H3BrClI
[MDL Number]

MFCD00672944
[MOL File]

31928-44-6.mol
[Molecular Weight]

317.35
Chemical PropertiesBack Directory
[Melting point ]

32-35℃
[Boiling point ]

279℃
[density ]

2.272
[Fp ]

123℃
[storage temp. ]

Room temperature.
[solubility ]

soluble in Methanol
[form ]

powder to lump to clear liquid
[color ]

White or Colorless to Yellow
[Sensitive ]

Light Sensitive
[InChI]

InChI=1S/C6H3BrClI/c7-5-3-4(8)1-2-6(5)9/h1-3H
[InChIKey]

CXHXFDQEFKFYQJ-UHFFFAOYSA-N
[SMILES]

C1(I)=CC=C(Cl)C=C1Br
[CAS DataBase Reference]

31928-44-6
Safety DataBack Directory
[Symbol(GHS) ]

Exclamation Mark (GHS07)
GHS07
[Signal word ]

Warning
[Hazard statements ]

H315-H319-H335
[Precautionary statements ]

P261-P280a-P304+P340-P305+P351+P338-P405-P501a
[Hazard Codes ]

Xi
[Risk Statements ]

36/37/38
[Safety Statements ]

26-37
[Hazard Note ]

Irritant
[HS Code ]

29039990
Spectrum DetailBack Directory
[Spectrum Detail]

2-Bromo-4-chloro-1-iodobenzene(31928-44-6)1HNMR
Hazard InformationBack Directory
[Synthesis]

2-Bromo-4-chloroaniline (10 g, 48 mmol) was suspended in hydrochloric acid water (50 mL of concentrated hydrochloric acid and 35 mL of water), and the suspension was cooled on a dry ice/methanol bath at -15°C. A sodium nitrite aqueous solution (3.6 g, 52 mmol, 1. 1 eq. /20 mL) was gradually added dropwise to it over 20 minutes, and the mixture was stirred from -15°C to 0°C for 30 minutes, thereby preparing a diazonium salt. The reaction solution was gradually added dropwise to a potassium iodide aqueous solution (73 g, 0.44 mol, 9 eq. /220 mL) at room temperature for 10 minutes. The reaction mixture was stirred at room temperature for 6 hours and then allowed to stand overnight. Dichloromethane (200 mL) was added to the reaction mixture, and subsequently, sodium hydrogensulfite (2 g) was added, deactivating the generated iodine. An organic layer was aliquoted, washed with a 10 % sodium hydrogensulfite aqueous solution (100 mL) and saturated salt water (30 mL) and dried over anhydrous magnesium sulfate. The solvent was then distilled off to obtain a red liquid. This was purified using column chromatography (silica gel/hexane) to obtain a white needle crystal 2-Bromo-4-chloro-1-iodobenzene (12.4 g, 81 %).
[References]

[1] Patent: EP2316816, 2011, A1. Location in patent: Page/Page column 21
[2] Chemistry - A European Journal, 2018, vol. 24, # 55, p. 14622 - 14626
[3] Angewandte Chemie - International Edition, 2008, vol. 47, # 5, p. 888 - 890
[4] Angewandte Chemie - International Edition, 2008, vol. 47, # 9, p. 1726 - 1728
[5] Journal of Organic Chemistry, 1987, vol. 52, # 5, p. 748 - 753
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