A facile synthesis of 3,4-dialkoxythiophenes

Synthetic Communications

Volumn 26, Issue 11, 1996, Pages 2205-2212

  Coffey, M ^a   McKellar, B R ^a   Reinhardt, B A ^b   Nijakowski, T ^c   Feld, W A ^a  

^a WRIGHT STATE UNIVERSITY   (United States)

^b AIR FORCE RESEARCH LABORATORY   (United States)

^c NONE

Author keywords

[No Author keywords available]

Indexed keywords

THIOPHENE DERIVATIVE;

ARTICLE; DRUG SYNTHESIS; INFRARED SPECTROPHOTOMETRY; MASS SPECTROMETRY; NUCLEAR MAGNETIC RESONANCE; REACTION ANALYSIS; TECHNIQUE;

EID: 0029955354     PISSN: 00397911     EISSN: None     Source Type: Journal    
DOI: 10.1080/00397919608003580     Document Type: Article

References (9)

1. a) Ledere, M., and Daoust, G., J. Chem. Soc.,Chem. Commun., 1990, 273.
2. b) Daoust, G. and Leclerc, M., Macromolecules, 1991, 24(2), 455.
3. Blohm, M.L., Van Dort, P.C., Pickett, J.E., Polym.Matl.Sci.Eng. Proc., 1991, 64, 210.
4. Kaeriyama, K., Masuda, H., Shirakawa, H., Akagi, K., Suezawa, H., Hirota, M., Polym.Matl.Sci.Eng.Proc., 1991, 64, 212.
5. Overberger, C.G., and Lai, J., J.Am.Chem.Soc., 1951, 73, 2956.
6. Groote, V.M., Tilak, B.D., Gadekar, K.N., and Sahasrabudhe, M.B., Tet., 1967, 23, 2443. It is imperative that 1 mole of diethyl oxalate, 1 mole of diethyl thiodigiycolate and 2 moles of sodium ethoxide be used in this condensation to get the yields reported.
7. Becker, H.J., and Stevens, W., Rec.Trav.Chim., 1940, 59, 435.
8. Dallacker, F., and Mues, V., Chem.Ber., 1975, 108, 569.
9. Guha, C., and lyer, B.H., J.Indian Inst.Sci., 1938, 21A, 115.