4-Bromo-1-(bromomethyl)-2-iodobenzene, alpha,4-Dibromo-2-iodotoluene

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4-Bromo-1-(bromomethyl)-2-iodobenzene, alpha,4-Dibromo-2-iodotoluene manufacturers

4-Bromo-1-(bromomethyl)-2-iodobenzene, alpha,4-Dibromo-2-iodotoluene Basic information
Product Name:4-Bromo-1-(bromomethyl)-2-iodobenzene, alpha,4-Dibromo-2-iodotoluene
Synonyms:4-Bromo-1-(bromomethyl)-2-iodobenzene, alpha,4-Dibromo-2-iodotoluene;4-Bromo-2-iodobenzyl bromide 97%;4-Bromo-2-iodobenzylbromide97%;4-Bromo-2-Iodobenzyl Bromide;Benzene, 4-bromo-1-(bromomethyl)-2-iodo-;4-Bromo-1-(bromomethyl)-2-iodobenzene
CAS:885681-96-9
MF:C7H5Br2I
MW:375.83
EINECS:
Product Categories:
Mol File:885681-96-9.mol
4-Bromo-1-(bromomethyl)-2-iodobenzene, alpha,4-Dibromo-2-iodotoluene Structure
4-Bromo-1-(bromomethyl)-2-iodobenzene, alpha,4-Dibromo-2-iodotoluene Chemical Properties
storage temp. 2-8°C(protect from light)
form crystalline powder
color Off white to cream
InChIInChI=1S/C7H5Br2I/c8-4-5-1-2-6(9)3-7(5)10/h1-3H,4H2
InChIKeyIHHHQROJDZQCQH-UHFFFAOYSA-N
SMILESC1(CBr)=CC=C(Br)C=C1I
Safety Information
HS Code 2903998090
MSDS Information
4-Bromo-1-(bromomethyl)-2-iodobenzene, alpha,4-Dibromo-2-iodotoluene Usage And Synthesis
Synthesis
4-BROMO-2-IODOTOLUENE

260558-15-4

4-Bromo-1-(bromomethyl)-2-iodobenzene, alpha,4-Dibromo-2-iodotoluene

885681-96-9

General procedure for the synthesis of 4-bromo-1-(bromomethyl)-2-iodobenzene (15b) from 4-bromo-2-iodo-1-methylbenzene: 4-bromo-2-iodotoluene (3.94 g, 13.3 mmol) was dissolved in 1,2-dichloroethane (19 mL) under nitrogen protection in a 50 mL two-necked round-bottomed flask and stirred at room temperature. Benzoyl peroxide (164 mg, 0.663 mmol) and N-bromosuccinimide (NBS, 2.63 g, 14.6 mmol) were then added sequentially and the reaction mixture was heated to reflux for 5 hours. After completion of the reaction, it was cooled to room temperature, the precipitate was collected by filtration and washed with hexane. The filtrate was dried over anhydrous magnesium sulfate (MgSO4), filtered and concentrated under reduced pressure to give an orange solid. The solid was washed with cold methanol to give an off-white solid product (3.27 g, 8.75 mmol, 66% yield), which could be used for subsequent reactions without further purification. The structure of the product was confirmed by 1H-NMR (400 MHz, CDCl3): δ 8.01 (d, 1H, J = 2.0 Hz), 7.47 (dd, 1H, J = 8.3, 2.0 Hz), 7.33 (d, 1H, J = 8.3 Hz), 4.54 (s, 2H); High-resolution Mass Spectrometry (HRMS, EI) m/z calculated value C7H5Br2I [M+]: 377.7762, measured value: 377.7759.

References[1] Patent: TW2016/9616, 2016, A. Location in patent: Paragraph 0162
[2] Journal of Organic Chemistry, 2011, vol. 76, # 7, p. 2227 - 2239
[3] Synthesis, 2011, # 15, p. 2387 - 2391
[4] Patent: WO2011/127383, 2011, A2. Location in patent: Page/Page column 74
[5] Angewandte Chemie - International Edition, 2014, vol. 53, # 7, p. 1841 - 1844
4-Bromo-1-(bromomethyl)-2-iodobenzene, alpha,4-Dibromo-2-iodotoluene Preparation Products And Raw materials
Raw materials4-BROMO-2-IODOTOLUENE-->N-Bromosuccinimide-->Benzoyl peroxide-->1,2-Dichloroethane
Tag:4-Bromo-1-(bromomethyl)-2-iodobenzene, alpha,4-Dibromo-2-iodotoluene(885681-96-9) Related Product Information
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