반응 #436325

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4-(diethylamino)salicylaldehyde

N-methyl-N-phenylhydrazine

4-(diethylamino)salicylaldehyde

→

4-(diethylamino)salicylaldehyde N-methyl-N-phenylhydrazone

수율 84.0%

용매

2-propanol

반응 조건

후처리

1. 1
   기타equipped with a reflux condenser and a magnetic stirrer
2. 2
   기타completely reacted
3. 3
   기타After the termination of the reaction
4. 4
   기타The crystals formed
5. 5
   여과were filtered
6. 6
   세척washed repeatedly with cold 2-propanol
7. 7
   기타dried under vacuum

실험 절차

A mixture of 4-(diethylamino)salicylaldehyde (10 g, 52 mmol, obtained from Aldrich) dissolved in 80 ml of 2-propanol, and N-methyl-N-phenylhydrazine (6.8 ml, 63 mmol, obtained from Aldrich) was added to a 250 ml round bottom flask equipped with a reflux condenser and a magnetic stirrer. The reaction mixture was refluxed until 4-(diethylamino)salicylaldehyde completely reacted. After the termination of the reaction, the reaction mixture was cooled to room temperature. The crystals formed were filtered and washed repeatedly with cold 2-propanol and dried under vacuum to yield 12.9 g (84%) of 4-(diethylamino)salicylaldehyde N-methyl-N-phenylhydrazone. The melting point was found to be 75.5–76.5° C. (recrystallized from 2-propanol). The 1H-NMR spectrum (100 Mhz) of the product in CDCl3 was characterized by the following chemical shifts (in ppm): 11.53 (s, 1H, OH); 7.63 (s, 1H, N═CH); 7.50–6.80 (m, 6H, Ar); 6.26 (m, 2H, Ar); 3.37 (m, 7H, CH2CH3, NCH3); 1.18 (t, 6H, CH2CH3, J=7.0 Hz). An elemental analysis yielded the following results in weight percent: C, 72.61; H, 7.88; N, 14.20, which compared with calculated values for C18H23N3O in weight percent of: C, 72.70; H, 7.80; N, 14.13.

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