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HRID 358926作成日:2026年10月26日

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

https://huagongshe.com/reaction/358926

反応式

関与物質

役割名称HCID仕込み量
反応物1,3,5-TrichlorobenzeneHCID 7950—
反応物2,4,6-TrinitrotolueneHCID 8376—
反応物TatbHCID 18286—
反応物Ar,ar,ar-trinitrobenzenetriamineHCID 6455494—
反応物PentanitroanilineHCID 11023554—
反応物TribromotrinitrobenzeneHCID 20067310—
生成物1,3,5-Trichloro-2,4,6-trinitrobenzeneHCID 17518—
生成物TatbHCID 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

DOI10.6084/m9.figshare.5104873.v1
特許番号US04997987
出典データセットuspto-grants-1991_03
ORD IDord-d13d80a5fa8947e5a80c18db3382a795
出典メモuspto-grants-1991_03