Identification | Back Directory | [Name]
1-ETHYNYL-2,6-DIMETHOXY-BENZENE | [CAS]
126829-31-0 | [Synonyms]
2,6-Dimethoxyphenylacetylene 1,3-Dimethoxy-2-ethynylbenzene 2-Ethynyl-1,3-diMethoxybenzene 1-ETHYNYL-2,6-DIMETHOXY-BENZENE Benzene, 2-ethynyl-1,3-diMethoxy- | [Molecular Formula]
C10H10O2 | [MDL Number]
MFCD08703538 | [MOL File]
126829-31-0.mol | [Molecular Weight]
162.19 |
Chemical Properties | Back Directory | [Melting point ]
106-108 °C | [Boiling point ]
265.1±30.0 °C(Predicted) | [density ]
1.06±0.1 g/cm3(Predicted) | [storage temp. ]
2-8°C | [Appearance]
Light brown to brown Solid |
Hazard Information | Back Directory | [Synthesis Reference(s)]
Tetrahedron Letters, 31, p. 6753, 1990 DOI: 10.1016/S0040-4039(00)97162-4 | [Synthesis]
GENERAL PROCEDURE: To a 25 mL round-bottomed flask, (2,6-dimethoxyphenyl)ethynyltrimethylsilane (1 mmol) and 5 mL of anhydrous tetrahydrofuran were added under nitrogen protection. Subsequently, tert-butylammonium fluoride (0.5 mmol) in 1 M tetrahydrofuran solution was slowly added to this solution. During the reaction, the colorless solution gradually changed to light to dark brown. The reaction mixture was stirred at room temperature for 2 hours. After completion of the reaction, silica gel (500 mg) was added to the mixture, followed by evaporation of the solvent under reduced pressure to obtain a silica gel plug. This silica plug was loaded on a silica gel column (2 cm × 5 cm) and eluted using hexane solution containing 5% ethyl acetate. The eluate corresponding to the product spot was collected and the solvent was evaporated under reduced pressure to finally obtain the target product 2-alkynyl-1,3-dimethoxybenzene. | [References]
[1] Bioorganic and Medicinal Chemistry, 2011, vol. 19, # 14, p. 4355 - 4365 [2] Advanced Synthesis and Catalysis, 2010, vol. 352, # 1, p. 201 - 211 [3] Organic Letters, 2014, vol. 16, # 3, p. 948 - 951 |
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