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HRID 358926Erstellt: 24. Oktober 2026

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

https://huagongshe.com/de/reaction/358926

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
Edukt1,3,5-TrichlorobenzeneHCID 7950—
Edukt2,4,6-TrinitrotolueneHCID 8376—
EduktTatbHCID 18286—
EduktAr,ar,ar-trinitrobenzenetriamineHCID 6455494—
EduktPentanitroanilineHCID 11023554—
EduktTribromotrinitrobenzeneHCID 20067310—
Produkt1,3,5-Trichloro-2,4,6-trinitrobenzeneHCID 17518—
ProduktTatbHCID 18286—

Reaktionsschritte

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.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS04997987
Quelldatensatzuspto-grants-1991_03
ORD IDord-d13d80a5fa8947e5a80c18db3382a795
Quellennotizuspto-grants-1991_03