Trietil ortoacetat je organsko jedinjenje sa formulom CH3C(OC2H5)3. To je etil ortoestar sirćetne kiseline. On je bezbojna uljasta tečnost.

Trietil ortoacetat
Skeletal formula of Triethylorthoacetate
Skeletal formula of Triethylorthoacetate
Ball-and-stick model of the Triethylorthoacetate molecule
Ball-and-stick model of the Triethylorthoacetate molecule
Nazivi
Preferisani IUPAC naziv
1,1,1-Trietoksietan
Identifikacija
3D model (Jmol)
ChemSpider
ECHA InfoCard 100.001.012
UNII
  • CCOC(C)(OCC)OCC
Svojstva
C8H18O3
Molarna masa 162,23 g·mol−1
Gustina 0,885 g/mL
Tačka ključanja 142 °C (288 °F; 415 K)
Ukoliko nije drugačije napomenuto, podaci se odnose na standardno stanje materijala (na 25 °C [77 °F], 100 kPa).
ДаY verifikuj (šta je ДаYНеН ?)
Reference infokutije

Trietil ortoacetat se koristi u organskoj sintezi za acetilaciju.[3] Takođe se koristi u Džonson-Klejzenovom rearanžiranju.[4]

Reference

уреди
  1. ^ Li Q, Cheng T, Wang Y, Bryant SH (2010). „PubChem as a public resource for drug discovery.”. Drug Discov Today. 15 (23-24): 1052—7. PMID 20970519. doi:10.1016/j.drudis.2010.10.003.  уреди
  2. ^ Evan E. Bolton; Yanli Wang; Paul A. Thiessen; Stephen H. Bryant (2008). „Chapter 12 PubChem: Integrated Platform of Small Molecules and Biological Activities”. Annual Reports in Computational Chemistry. 4: 217—241. doi:10.1016/S1574-1400(08)00012-1. 
  3. ^ B. W. Howk, J. C. Sauer (1959). „Phenylpropargylaldehyde Diethyl Acetal”. Organic Syntheses. 39: 59. doi:10.15227/orgsyn.039.0059. 
  4. ^ Fernandes, Rodney A.; Chowdhury, Asim K.; Kattanguru, Pullaiah (2014). „The Orthoester Johnson-Claisen Rearrangement in the Synthesis of Bioactive Molecules, Natural Products, and Synthetic Intermediates - Recent Advances”. European Journal of Organic Chemistry. 2014 (14): 2833—2871. doi:10.1002/ejoc.201301033.