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1-Ethyl-4-iodobenzene

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1-Ethyl-4-iodobenzene Basic information
Product Name:1-Ethyl-4-iodobenzene
Synonyms:4-ETHYLIODOBENZENE;P-ETHYLIODOBENZENE;4-Iodoethylbenzene;1-Ethyl-4-iodobenzene,99%;p-Iodoethylbenzene;4-Iodo-1-ethylbenzene; Benzene, 1-ethyl-4-iodo-;1-Ethyl-4-iodobenzene
CAS:25309-64-2
MF:C8H9I
MW:232.06
EINECS:607-691-3
Product Categories:Iodine Compounds;Aryl;C8;Halogenated Hydrocarbons
Mol File:25309-64-2.mol
1-Ethyl-4-iodobenzene Structure
1-Ethyl-4-iodobenzene Chemical Properties
Melting point -17 °C
Boiling point 112-113 °C (20 mmHg)
density 1,6 g/cm3
refractive index 1.5905-1.5925
Fp 107 °C
storage temp. Keep in dark place,Sealed in dry,Room Temperature
form liquid
Specific Gravity1.6
color Yellow
Sensitive Light Sensitive
BRN 2076973
CAS DataBase Reference25309-64-2(CAS DataBase Reference)
Safety Information
Hazard Codes Xi,C
Risk Statements 36/38-36
Safety Statements 37/39-26-36
HS Code 29036990
MSDS Information
ProviderLanguage
ACROS English
ALFA English
1-Ethyl-4-iodobenzene Usage And Synthesis
Chemical Propertiesclear colorless to yellow liquid
Synthesis
Ethylbenzene

100-41-4

1-ETHYL-4-IODOBENZENE

25309-64-2

GENERAL STEPS: To a solution of 1,2-dimethylbenzene (0.106 g, 1 mmol) in acetonitrile (10 mL) was sequentially added iodine (1 mmol, 0.126 g) and polymer-loaded periodate (0.6 g, 1.05 mmol). The reaction mixture was stirred at 40 °C for 1 hour. The progress of the reaction was monitored by thin layer chromatography (TLC) and the unfolding agent was a solvent mixture of ethyl acetate and hexane (1:9, v/v). After completion of the reaction, the mixture was cooled to room temperature and filtered. Excess iodine in the filtrate was quenched by adding sodium bisulfite solution (1 M) dropwise. The organic layer was separated, dried with anhydrous magnesium sulfate, filtered and concentrated under reduced pressure to remove the solvent. The crude product was purified by silica gel column chromatography, eluting with a mixed solvent gradient of hexane and ethyl acetate to give 1-ethyl-4-iodobenzene in 95% isolated yield with a boiling point of 235 °C (literature value: 234 °C).

References[1] Bulletin of the Chemical Society of Ethiopia, 2014, vol. 28, # 2, p. 305 - 308
[2] Journal of applied chemistry of the USSR, 1984, vol. 57, # 1 pt 2, p. 121 - 123
[3] Journal fuer Praktische Chemie (Leipzig), 1902, vol. <2> 65, p. 568
[4] Journal of the Indian Chemical Society, 1936, vol. 13, p. 187
[5] Journal of the Indian Chemical Society, 1937, vol. 14, p. 157
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