関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|
| 反応物 | 1,3,5-Trichlorobenzene | HCID 7950 | — |
| 反応物 | 2,4,6-Trinitrotoluene | HCID 8376 | — |
| 反応物 | Tatb | HCID 18286 | — |
| 反応物 | Ar,ar,ar-trinitrobenzenetriamine | HCID 6455494 | — |
| 反応物 | Pentanitroaniline | HCID 11023554 | — |
| 反応物 | Tribromotrinitrobenzene | HCID 20067310 | — |
| 生成物 | 1,3,5-Trichloro-2,4,6-trinitrobenzene | HCID 17518 | — |
| 生成物 | Tatb | HCID 18286 | — |
反応手順
Triaminotrinitrobenzene is an explosive having unusual insensitivity, stability at high temperature, and respectable performance. It is insoluble in organic solvents and has a melting point above 400° C. TATB was prepared in 1887 from tribromotrinitrobenzene. It has also been prepared on a laboratory scale from 2,4,6-trinitrotoluene through selective reduction of the 4-nitro group, nitration to pentanitroaniline, and then ammonolysis. Currently, the manufacture of TATB (1) on a large scale begins with 1,3,5-trichlorobenzene (TCB, 2) which is nitrated to give 1,3,5-trichloro-2,4,6-trinitrobenzene (TCTNB, 3) as shown in FIGS. 1a and 1b hereof. The nitration step requires severe conditions of high temperature, long reaction time, and oleum, and results in significant quantities of by-products.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 特許番号 | US04997987 |
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| 出典データセット | uspto-grants-1991_03 |
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| ORD ID | ord-d13d80a5fa8947e5a80c18db3382a795 |
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| 出典メモ | uspto-grants-1991_03 |
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