2,6-DIBROMO-1,5-DIHYDROXYNAPHTHALENE
2,6-DIBROMO-1,5-DIHYDROXYNAPHTHALENE Basic information
- Product Name:
- 2,6-DIBROMO-1,5-DIHYDROXYNAPHTHALENE
- Synonyms:
-
- 2,6-dibromo-5-naphthalenediol
- 2,6-dibromonaphthalene-1,5-diol
- 2,6-DIBROMO-1,5-DIHYDROXYNAPHTHALENE
- 2,6-DIBROMO-1,5-NAPHTHALENEDIOL
- 1,5-DIHYDROXY-2,6-DIBROMONAPHTHALENE
- 2,6-Dibromo-1,5-dihydroxynaphthalene>
- 1,5-Naphthalenediol, 2,6-dibromo-
- CAS:
- 84-59-3
- MF:
- C10H6Br2O2
- MW:
- 317.96
- EINECS:
- 201-543-8
- Mol File:
- 84-59-3.mol
2,6-DIBROMO-1,5-DIHYDROXYNAPHTHALENE Chemical Properties
- Boiling point:
- 397.4±37.0 °C(Predicted)
- Density
- 2.081±0.06 g/cm3(Predicted)
- storage temp.
- Sealed in dry,Room Temperature
- form
- powder to crystal
- pka
- 6.19±0.50(Predicted)
- color
- Light yellow to Amber to Dark green
- CAS DataBase Reference
- 84-59-3(CAS DataBase Reference)
Safety Information
- Risk Statements
- 36/37/38
- Safety Statements
- 26-36/37/39
- HS Code
- 2908.19.6000
2,6-DIBROMO-1,5-DIHYDROXYNAPHTHALENE Usage And Synthesis
Uses
2,6-Dibromo-1,5-naphthalenediol is a useful synthetic intermediate. It is used to prepare semiconducting polyphenyls and polythiophenes via microwave-assisted Suzuki and Stille cross-coupling reactions. It is also used to prepare and polymerize adamantane or phenylenevinylene or naphthalenevinylene-containing monomers.
Synthesis
83-56-7
84-59-3
Example 17- Synthesis of 2,6-dibromonaphthalene-1,5-diol: 1,5-dihydroxynaphthalene (115.2 g) was suspended in acetonitrile (800 mL) under nitrogen protection. Subsequently, N,N-dimethylformamide (DMF) solution of N-bromosuccinimide (NBS) (400 mL containing 254 g of NBS) was added slowly and dropwise. The reaction mixture was stirred at room temperature and the reaction progress was monitored by gas chromatography-mass spectrometry (GC-MS). Upon completion of the reaction, the reaction was quenched by the addition of water. The resulting precipitate was collected by filtration and washed with plenty of water to give 2,6-dibromonaphthalene-1,5-diol in 80% yield. Mass spectrometry (electrospray ionization, ESI) analysis resulted in a calculated value (C10H6Br2O2) of 317.9614 and a measured value of 317.9.
References
[1] Journal of Organic Chemistry, 2017, vol. 82, # 15, p. 8234 - 8241
[2] Patent: US2011/224445, 2011, A1. Location in patent: Page/Page column 19
[3] Patent: WO2013/149001, 2013, A2. Location in patent: Paragraph 00139
[4] Tetrahedron Letters, 2017, vol. 58, # 40, p. 3854 - 3858
[5] Organic Electronics: physics, materials, applications, 2014, vol. 15, # 12, p. 3558 - 3567
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