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Preferred IUPAC name 4-Ethynylbenzaldehyde | |
Other names p-Ethynylbenzaldehyde | |
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CAS Number | |
3D model (JSmol) | |
ChemSpider | |
ECHA InfoCard | 100.155.717 |
EC Number |
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PubChem CID | |
CompTox Dashboard (EPA) | |
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Properties | |
Chemical formula | C9H6O |
Molar mass | 130.146 g·mol |
Appearance | white or yellow solid |
Melting point | 89–93 °C (192–199 °F; 362–366 K) |
Except where otherwise noted, data are given for materials in their standard state (at 25 °C , 100 kPa). Infobox references |
4-Ethynylbenzaldehyde, or p-ethynylbenzaldehyde, is an organic compound with the formula HC2C6H4COH. It is an ethynyl derivative of benzaldehyde, or may also be viewed as a formylated derivative of phenylacetylene.
Preparation
4-Ethynylbenzaldehyde may be prepared by the Sonogashira coupling of 4-bromobenzaldehyde with trimethylsilylacetylene to form 4-((trimethylsilyl)ethynyl)benzaldehyde, followed by removal of the trimethylsilyl group with base to form 4-ethynylbenzaldehyde.
Reactions
The ethynyl functionality of 4-ethynylbenzaldehyde may undergo a Sonogashira coupling with another molecule of 4-bromobenzaldehyde to form the symmetrical dialdehyde 4,4'-(ethyne-1,2-diyl)dibenzaldehyde.
References
- "4-Ethynylbenzaldehyde". ChemSpider. Retrieved 21 October 2023.
- PubChem. "4-Ethynylbenzaldehyde". pubchem.ncbi.nlm.nih.gov. Retrieved 2023-10-22.
- ^ Xu, X.; Cai, P.; Chen, H.; Zhou, H.-C.; Huang, N. (28 September 2022). "Three-Dimensional Covalent Organic Frameworks with she Topology". Journal of the American Chemical Society. 144 (40): 18511–18517. doi:10.1021/jacs.2c07733. PMID 36170014. S2CID 252566430.