HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1742116Generated: November 3, 2026
4-Chloro-3,5-dinitrobenzotrifluoride → 5-(Trifluoromethyl)benzene-1,3-diamine
https://huagongshe.com/reaction/1742116
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 4-Chloro-3,5-dinitrobenzotrifluoride | HCID 9809 | — |
| Reactant | 2,3-Diaminobenzotrifluoride | HCID 436759 | — |
| Reactant | Sodium Acetate | HCID 517045 | — |
| Reactant | Sodium Formate | HCID 2723810 | — |
| Catalyst | Palladium | HCID 23938 | — |
| Solvent | Acetic Acid | HCID 176 | — |
| Product | 5-(Trifluoromethyl)benzene-1,3-diamine | HCID 67781 | 45% |
Reaction Steps
Sodium formate (12.24 g) was added to a mixture of 4-chloro-3,5-dinitrobenzotrifluoride (5.41 g), sodium acetate (1.64 g) and 5% Pd/C (0.5 g) in glacial acetic acid (60 mL). The mixture was stirred and the resultant exotherm, which lasted about an hour, was controlled by cooling to maintain a reaction temperature of about 40° C. As the exotherm subsided, external heating was applied to maintain the temperature at about 40° C. Gas chromatographic analysis of the reaction mixture, at the end of one hour, indicated diaminobenzotrifluoride as the major component (35%) with no 4-chloro-3,5-dinitrobenzotrifluoride remaining. The maximum amount (about 45%) of 3,5-diaminobenzotrifluoride formed after 2 hours after which it was converted to other undesirable products.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05336808 |
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| Source dataset | uspto-grants-1994_08 |
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| ORD ID | ord-185781839bed40fca10d6de331075990 |
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| Source note | uspto-grants-1994_08 |
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