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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 358926생성일: 2026년 10월 25일

1,3,5-Trichlorobenzene → 1,3,5-Trichloro-2,4,6-trinitrobenzene

https://huagongshe.com/reaction/358926

반응식

참여 물질

역할이름HCID투입량
반응물1,3,5-TrichlorobenzeneHCID 7950—
반응물2,4,6-TrinitrotolueneHCID 8376—
반응물TatbHCID 18286—
반응물Ar,ar,ar-trinitrobenzenetriamineHCID 6455494—
반응물PentanitroanilineHCID 11023554—
반응물TribromotrinitrobenzeneHCID 20067310—
생성물1,3,5-Trichloro-2,4,6-trinitrobenzeneHCID 17518—
생성물TatbHCID 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

DOI10.6084/m9.figshare.5104873.v1
특허 번호US04997987
출처 데이터셋uspto-grants-1991_03
ORD IDord-d13d80a5fa8947e5a80c18db3382a795
출처 메모uspto-grants-1991_03