Department of Chemistry, Shiraz University, Zip code 71454, Shiraz, I.R. IRAN
10.30492/ijcce.1999.10476
Abstract
The reaction of tertiary, secondary and benzylic alcohols with different nitriles in the presence of alumina-methanesulfonic acid (AMA) as a new reagent affords the corresponding amides in good yields (Table 1, 2). Conversion of 2,6-bis(hydroxymethyl)-4-halo anisoles into corresponding diamides in the range of 68-76% yields (Table 3) are also included in this paper.
Sharghi, H., & Niknam, K. (1999). Conversion of Alcohols into Amides Using Alumina-Methanesulfonic Acid (AMA) in Nitrile Solvents. Iranian Journal of Chemistry and Chemical Engineering, 18(1), 36-39. doi: 10.30492/ijcce.1999.10476
MLA
Hashem Sharghi; Khodabakhsh Niknam. "Conversion of Alcohols into Amides Using Alumina-Methanesulfonic Acid (AMA) in Nitrile Solvents". Iranian Journal of Chemistry and Chemical Engineering, 18, 1, 1999, 36-39. doi: 10.30492/ijcce.1999.10476
HARVARD
Sharghi, H., Niknam, K. (1999). 'Conversion of Alcohols into Amides Using Alumina-Methanesulfonic Acid (AMA) in Nitrile Solvents', Iranian Journal of Chemistry and Chemical Engineering, 18(1), pp. 36-39. doi: 10.30492/ijcce.1999.10476
VANCOUVER
Sharghi, H., Niknam, K. Conversion of Alcohols into Amides Using Alumina-Methanesulfonic Acid (AMA) in Nitrile Solvents. Iranian Journal of Chemistry and Chemical Engineering, 1999; 18(1): 36-39. doi: 10.30492/ijcce.1999.10476