참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | 1,3,5-Trichlorobenzene | HCID 7950 | — |
| 반응물 | 2,4,6-Trinitrotoluene | HCID 8376 | — |
| 반응물 | Tatb | HCID 18286 | — |
| 반응물 | Ar,ar,ar-trinitrobenzenetriamine | HCID 6455494 | — |
| 반응물 | Pentanitroaniline | HCID 11023554 | — |
| 반응물 | Tribromotrinitrobenzene | HCID 20067310 | — |
| 생성물 | 1,3,5-Trichloro-2,4,6-trinitrobenzene | HCID 17518 | — |
| 생성물 | Tatb | HCID 18286 | — |
반응 단계
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.
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US04997987 |
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| 출처 데이터셋 | uspto-grants-1991_03 |
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| ORD ID | ord-d13d80a5fa8947e5a80c18db3382a795 |
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| 출처 메모 | uspto-grants-1991_03 |
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