A new, three-stage synthesis of 1,3,5-triamino-2,4,6-trinitrobenzene (TATB) has been developed which avoids the use of halogenated precursors or reagents. The starting material, 1,3,5trihydroxy-benzene, is converted via the sequence nitrationalkylation-amination to TATB in an overall yield of 87%. T
β¦ LIBER β¦
A new route to 5-trifluoromethyl-2,3-dihydro-1,4-diazepine and 2-trifluoromethylbenzimidazole
β Scribed by Shizheng Zhu; Qianli Chu; Yanli Wang
- Publisher
- John Wiley and Sons
- Year
- 2000
- Tongue
- English
- Weight
- 165 KB
- Volume
- 11
- Category
- Article
- ISSN
- 1042-7163
No coin nor oath required. For personal study only.
β¦ Synopsis
Ethylenediamine reacted readily with 4ethoxy-1,1,1-trifluoro-3-butene-2-one to form 5-trifliuoromethyl-2,3-dihydro-1,4-diazepine in good yield. Under the same reaction conditions, o-phenylenediamine gave 2-trifluoromethylbenzimidazole and benzimidazole.
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