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1646-54-4

1646-54-4 Structure

1646-54-4 Structure
IdentificationBack Directory
[Name]

1,4-DIBROMO-2,3,5,6-TETRAMETHYLBENZENE
[CAS]

1646-54-4
[Synonyms]

Dibromodurene
3,6-Dibromodurene
1,4-Dibromodurene
6-TETRAMETHYLBENZENE
1,4-Dibromotetramethylbenzene
4,6-Dibromo-1,2,4,5-tetramethylbenzene
3,6-Dibromo-1,2,4,5-tetramethylbenzene
1,4-DIBROMO-2,3,5,6-TETRAMETHYLBENZENE
1,2,4,5-Tetramethyl-3,6-dibromobenzene
Benzene,1,4-dibroMo-2,3,5,6-tetraMethyl-
2,3,5,6-Tetramethyl-1,4-phenylene dibromide
[Molecular Formula]

C10H12Br2
[MDL Number]

MFCD00017787
[MOL File]

1646-54-4.mol
[Molecular Weight]

292.01
Chemical PropertiesBack Directory
[Melting point ]

202-204 °C
[Boiling point ]

307.7±37.0 °C(Predicted)
[density ]

1.562±0.06 g/cm3(Predicted)
[storage temp. ]

Sealed in dry,Room Temperature
[solubility ]

soluble in Toluene
[form ]

powder to crystal
[color ]

White to Almost white
[EPA Substance Registry System]

Benzene, 1,4-dibromo-2,3,5,6-tetramethyl- (1646-54-4)
Safety DataBack Directory
[Hazard statements ]

H413
[TSCA ]

TSCA listed
[HS Code ]

2903.99.8001
Spectrum DetailBack Directory
[Spectrum Detail]

1,4-DIBROMO-2,3,5,6-TETRAMETHYLBENZENE(1646-54-4)1HNMR
Hazard InformationBack Directory
[Synthesis]

1,2,4,5-Tetramethylbenzene

95-93-2

1,4-DIBROMO-2,3,5,6-TETRAMETHYLBENZENE

1646-54-4

1. 1,2,4,5-tetramethylbenzene (25.0 g, 0.18 mol) and 150 mL of methylene chloride were added to a dry three-necked flask with stirring until completely dissolved. 2. Iodine (I2, 1.0 g, 3.94 mmol) was added to the solution as a catalyst. 3. Under stirring, bromine (Br2, 24 mL, 74.6 g, 0.47 mol) dissolved in a 100 mL of dichloromethane. 4. After the dropwise addition was completed, the reaction mixture was heated to reflux and held for 1.5 h. 5. After the reaction was completed, it was cooled to room temperature and the reaction was quenched by the addition of 5 M aqueous sodium hydroxide (50 mL). 6. The solid product was collected by filtration, washed with deionized water, and dried to afford 1,4-dibromo-2,3,5,6-tetramethylbenzene in 93% yield ( The product was characterized by 1H NMR (500 MHz, CDCl3) and 13C NMR (125.68 MHz, CDCl3): 1H NMR δ 2.48 (s, 12H); 13C NMR δ 135.2, 128.3, 22.4. 8. The 1H NMR spectrum and structure of the product are shown in Figure 1.

[References]

[1] Patent: KR2015/112649, 2015, A. Location in patent: Paragraph 0110-0112
[2] Patent: US2011/130593, 2011, A1. Location in patent: Page/Page column 6
[3] Angewandte Chemie - International Edition, 2016, vol. 55, # 9, p. 3049 - 3053
[4] Angew. Chem., 2016, vol. 128, # 9, p. 3101 - 3105,5
[5] Bulletin of the Chemical Society of Japan, 1989, vol. 62, # 2, p. 439 - 443
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