Adding a certain compound to certain chemical reactions, such as: 36556-42-0, name is 1-Chloro-2,3,4-trifluorobenzene, belongs to chlorides-buliding-blocks compound, can increase the reaction rate and produce products with better performance than those obtained under traditional synthetic methods. Here is a downstream synthesis route of the compound 36556-42-0, Quality Control of 1-Chloro-2,3,4-trifluorobenzene
The amine mother liquor, together with the production residues from the initial batch, is made up with 299.7 g (1.8 mol) of 4-chloro-1,2,3-trifluorobenzene and 4.1 g of 5% Pd/C (50% water-moist) and, analogously to the initial batch, is reductively dechlorinated and worked up correspondingly. The production residues resulting from the fractionation (forerunnings, intermediate runnings and residues from distillation) are recycled without further pretreatment to the subsequent batch. Conversion: 98.1% (by GC) Yield: 231.0 g (1.75 mol) of 1,2,3-trifluorobenzene 97.2% based on the 4-chloro-1,2,3-trifluorobenzene employed. Purity: >99.9 (GC area-%) 1,2,3-trifluorobenzene
In the field of chemistry, the synthetic routes of compounds are constantly being developed and updated. I will also mention this compound in other articles, 1-Chloro-2,3,4-trifluorobenzene, other downstream synthetic routes, hurry up and to see.
Reference:
Patent; Hoechst Aktiengesellschaft; US5498807; (1996); A;,
Chloride – Wikipedia,
Chlorides – an overview | ScienceDirect Topics