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3,5-Bis[5-(4-tert-butylphenyl)-1,3,4-oxadiazol-2-yl]nitrobenzene
 
 
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Short Note

3,5-Bis[5-(4-tert-butylphenyl)-1,3,4-oxadiazol-2-yl]benzenamine

by
Frank Osterod
and
Arno Kraft
*,*
Department of Organic Chemistry and Macromolecular Chemistry II, University of Düsseldorf, Universitätsstr. 1, D-40225 Düsseldorf, Germany
*
Author to whom correspondence should be addressed.
*
New address: Department of Chemistry, Heriot-Watt University, Riccarton, Edinburgh EH14 4AS, UK.
Molecules 1999, 4(10), M115; https://doi.org/10.3390/M115
Submission received: 15 September 1999 / Accepted: 15 September 1999 / Published: 8 October 1999
(This article belongs to the Section Molbank Section of Molecules, 1997-2001)
Versions Notes
Molecules 04 m115 i001
The reduction was carried out as described in reference [1] by using a mixture of sulfur (7.10 g, 0.22 mol), Na2S — 9 H2O (240 g, 0.22 mol), water (140 mL) and pyridine (20 mL). A solution of this reducing agent (60 mL) was added to a solution of 3,5-bis[5-(4-tert-butylphenyl)-1,3,4-oxadiazol-2-yl]nitrobenzene (1) (1.00 g, 1.9 mmol) in warm pyridine (10 mL). The reaction mixture was heated to reflux for 90 min, during which time a yellow precipitate separated. The mixture was filtered and the filtrate was added dropwise to water (200 mL). The precipitate was collected by suction filtration and dried. The combined solids were extracted with chloroform, the solution was filtered and concentrated in vacuum to yield 2 as a light yellow solid (260 mg, 28%). The yield was not optimised [2].
Mp. : 291-293°C.
IR (KBr): 3357s; 2964s; 1616m; 1543m; 1495s; 1464m; 1458m; 1114w; 1011w; 842w; 726w.
1H NMR (CDCl3:DMSO-d6 6:1, 300 MHz): 8.09 (t, J = 1.4 Hz, 1 H, C6H3); 8.09 (AA′XX′, 4 H, C6H4); 7.65 (d, J = 1.4 Hz, 2 H, C6H3); 7.59 (AA′XX′, 4 H, C6H4); 4.92 (br. s, 2 H, NH2); 1.39 (s, 18 H, CH3).
13C NMR (CDCl3:DMSO-d6 7:3, 125 MHz): 164.4; 163.8; 155.2; 149.4; 126.6; 126.04; 126.0; 125.2; 120.7; 114.8; 34.9; 31.0.
CI-MS (NH3) : 512 (35); 511 (100, M+NH4+); 495 (28); 494 (78, M+H+); 194 (36); 177 (28).

Reference and Notes

  1. Krasovitskii, B. M.; Matskevich, R. M.; Malt'seva, N. I. J. Gen. Chem. USSR 1961, 2107.
  2. The reduction procedure worked reasonably well and provided the only successful way to the amine. Other reduction conditions [formic acid, NEt3, Pd/C; hydrazine hydrate, Raney-Ni; carbon monoxide, SnCl4, PtCl2(PPh3)2, dioxane] failed completely. However, considerable amounts of H2S evolved during the reaction; because of the stench involved, we decided in the end not to repeat the procedure a second time.
Sample availability: available from the authors.

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MDPI and ACS Style

Osterod, F.; Kraft, A. 3,5-Bis[5-(4-tert-butylphenyl)-1,3,4-oxadiazol-2-yl]benzenamine. Molecules 1999, 4, M115. https://doi.org/10.3390/M115

AMA Style

Osterod F, Kraft A. 3,5-Bis[5-(4-tert-butylphenyl)-1,3,4-oxadiazol-2-yl]benzenamine. Molecules. 1999; 4(10):M115. https://doi.org/10.3390/M115

Chicago/Turabian Style

Osterod, Frank, and Arno Kraft. 1999. "3,5-Bis[5-(4-tert-butylphenyl)-1,3,4-oxadiazol-2-yl]benzenamine" Molecules 4, no. 10: M115. https://doi.org/10.3390/M115

APA Style

Osterod, F., & Kraft, A. (1999). 3,5-Bis[5-(4-tert-butylphenyl)-1,3,4-oxadiazol-2-yl]benzenamine. Molecules, 4(10), M115. https://doi.org/10.3390/M115

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