2,5-Dimethoxynaphthalene
2,5-Dimethoxynaphthalene Basic information
- Product Name:
- 2,5-Dimethoxynaphthalene
- Synonyms:
-
- 1,6-DIMETHOXYNAPHTHALENE, 98+%
- 2,5(1,6)-Dimethoxy Naphthalene
- 1,6-DimethoxylNaphthalene
- 1,6-DIMETHOXYNAPHTHALENE
- 2,5-DIMETHOXY NAPHTHALENE
- 3,8-DiMethoxynaphthalene
- NSC 167477
- Naphthalene, 1,6-diMethoxy-
- CAS:
- 3900-49-0
- MF:
- C12H12O2
- MW:
- 188.22
- Product Categories:
-
- Ethers
- Organic Building Blocks
- Oxygen Compounds
- Aromatics
- Intermediates
- Intermediates of Dyes and Pigments
- FINE Chemical & INTERMEDIATES
- Naphthalene derivatives
- Mol File:
- 3900-49-0.mol
2,5-Dimethoxynaphthalene Chemical Properties
- Melting point:
- 56-60 °C(lit.)
- Boiling point:
- 123°C 0,8mm
- Density
- 1.097±0.06 g/cm3(Predicted)
- Flash point:
- 123°C/0.8mm
- storage temp.
- Sealed in dry,Room Temperature
- solubility
- Chloroform, Dichloromethane
- form
- Solid
- color
- Brown
- BRN
- 1945987
- CAS DataBase Reference
- 3900-49-0(CAS DataBase Reference)
MSDS
- Language:English Provider:SigmaAldrich
- Language:English Provider:ALFA
2,5-Dimethoxynaphthalene Usage And Synthesis
Chemical Properties
Brown Solid
Uses
Intermediate in the production of tetralin derivatives
Synthesis
575-44-0
74-88-4
3900-49-0
In a round-bottomed flask equipped with a magnetic stirrer, 1.6 g (10.0 mmol) of 1,6-dihydroxynaphthalene (compound 39, purchased from Tokyo Chemical Industry Co., Ltd.) was dissolved in 15 mL of N,N-dimethylformamide (DMF). Subsequently, 14.2 g (100.0 mmol) of iodomethane (purchased from Wako Pure Chemical Industries, Ltd.) and 13.8 g (100.0 mmol) of potassium carbonate (purchased from Wako Pure Chemical Industries, Ltd.) were added to the solution. The reaction mixture was stirred at room temperature for 2 hours. After completion of the reaction, the reaction mixture was extracted by adding dichloromethane and water to the reaction mixture and the organic layer was separated and washed with distilled water. The solvent was removed by distillation under reduced pressure to give 1.7 g (yield: 90%) of 2,5-dimethoxynaphthalene (compound 40) as a colorless liquid.
References
[1] Patent: US2017/342031, 2017, A1. Location in patent: Paragraph 0643
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