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ChemicalBook--->CAS DataBase List--->38846-64-9

38846-64-9

38846-64-9 Structure

38846-64-9 Structure
IdentificationBack Directory
[Name]

2-ETHYNYLBENZALDEHYDE
[CAS]

38846-64-9
[Synonyms]

2-ETHYNYLBENZALDEHYDE
2-Formylphenylacetylene
Benzaldehyde, 2-ethynyl-
2-Ethynylbenzaldehyde97%
2-Ethynylbenzaldehyde 97%
2-ETHYLNYLBENZALDEHYDE, 97%
Benzaldehyde, 2-ethynyl- (9CI)
[Molecular Formula]

C9H6O
[MDL Number]

MFCD04039985
[MOL File]

38846-64-9.mol
[Molecular Weight]

130.14
Chemical PropertiesBack Directory
[Melting point ]

64-67 °C (lit.)
[Boiling point ]

115 °C(Press: 12 Torr)
[density ]

1.07±0.1 g/cm3(Predicted)
[storage temp. ]

Keep in dark place,Sealed in dry,Room Temperature
[form ]

solid
[color ]

Light yellow to light brown
[InChIKey]

ZEDSAJWVTKUHHK-UHFFFAOYSA-N
Safety DataBack Directory
[Symbol(GHS) ]


GHS07
[Signal word ]

Warning
[Hazard statements ]

H315-H319-H335
[Precautionary statements ]

P261-P264-P271-P280-P302+P352-P305+P351+P338
[Hazard Codes ]

Xi,F
[Risk Statements ]

36/37/38
[Safety Statements ]

26-36
[WGK Germany ]

3
[HS Code ]

2912290090
Hazard InformationBack Directory
[Uses]

2-Ethynylbenzaldehyde may be used in the synthesis of the following:
  • iodoisoquinoline-fused benzimidazoles obtained via tandem iodocyclization of 2-ethynylbenzaldehyde with o-benzenediamine and iodine in the presence of copper(I)iodide
  • N-[(7,7a-dihydroisoquinolino[2,1-a]perimidin-13-yl)methyl]-N-isopropylpropan-2-amine obtained via a multi-step process
It may also be used in the synthesis of the following substituted 2-alkynylbenzaldehydes by Sonogashira coupling:
  • 2-[(2-bromophenyl)ethynyl]benzaldehyde
  • 2-[(2-bromo-5-fluorophenyl)ethynyl]benzaldehyde
  • 2-[(2-bromo-5-methylphenyl)ethynyl]benzaldehyde
  • 2-(phenylethynyl)benzaldehyde
  • 2-[(4-methylphenyl)ethynyl]benzaldehyde
[Synthesis]

2-(TRIMETHYLSILYL)ETHYNYLBENZALDEHYDE

77123-58-1

2-ETHYNYLBENZALDEHYDE

38846-64-9

General procedure for the synthesis of 2-ethynylbenzaldehyde from 2-[(trimethylmethylsilyl)ethynyl]benzaldehyde: 2-[(trimethylmethylsilyl)ethynyl]benzaldehyde (1 mmol), an inorganic base (potassium tert-butanol, sodium tert-butanol, potassium hydroxide, sodium hydroxide, or potassium trimethylmethylsilyl, sodium trimethylmethylsilyl, 0.05 mmol), and 2 mL of DMA or DMSO solvent were added to a 10mL sealed tube. The mixture was placed in an oil bath at 60 °C and the reaction was stirred for 12 h. The progress of the reaction was monitored by TLC. Upon completion of the reaction, equal amounts of homotrimethylbenzene or n-undecane were added as an internal standard for the crude product, and the exact yield of the product was determined by GC and GC-MS analysis. According to the results of GC and GC-MS analyses, when DMSO was used as the reaction solvent and potassium tert-butanol, sodium tert-butanol, potassium hydroxide, sodium hydroxide, or potassium trimethylmethylsilyl, sodium trimethylmethylsilyl were used as catalysts, the yields of the products were 44%, 47%, 49%, 50%, 77%, and 70% respectively. When DMA was used as the reaction solvent with the same inorganic base as the catalyst, the yields of the products were 40%, 42%, 42%, 40%, 61%, 59%, respectively.

[References]

[1] Synthesis, 2010, # 14, p. 2367 - 2378
[2] European Journal of Organic Chemistry, 2017, vol. 2017, # 11, p. 1425 - 1433
[3] Journal of the Chemical Society, Perkin Transactions 1: Organic and Bio-Organic Chemistry (1972-1999), 1987, p. 2321 - 2332
[4] Advanced Synthesis and Catalysis, 2011, vol. 353, # 2-3, p. 392 - 400
[5] Journal of the American Chemical Society, 2015, vol. 137, # 9, p. 3233 - 3236
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