HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1450023Generated: November 2, 2026
Trifluoromethyl toluidine → 5-Chloro-2-methylbenzotrifluoride
https://huagongshe.com/reaction/1450023
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Trifluoromethyl toluidine | HCID 2735932 | — |
| Reactant | HCID 10890716 | HCID 10890716 | — |
| Reactant | HCID 10966608 | HCID 10966608 | — |
| Product | 5-Chloro-2-methylbenzotrifluoride | HCID 11790101 | — |
Reaction Steps
2-Trifluoromethyl-4-chloro-benzalchloride and 2-methyl-3-nitro-5-chlorobenzotrifluoride, are intermediates in a process of preparing 2-methyl-3-aminobenzo-trifluoride. In this process, 2-trifluoromethyl-4-chlorobenzal-chloride is prepared by chlorinating o-trifluoromethylbenzalhalide, and 2-methyl-3-nitro-5-chlorobenzotrifluoride is prepared at first by hydrogenating the 2-trifluoro-methyl-4-chlorobenzalhalide to form a 2-methyl-5-monochlorobenzotrifluoride and then by nitrating the 2-methyl-5-monochlorobenzotrifluoride. Following this process, 2-methyl-3-aminobenzotrifluoride (MA-BTF) is prepared by hydrogenating the 2-methyl-3-nitro-5-chlorobenzotrifluoride. The thus prepared 2-methyl-3-aminobenzotrifluoride is useful as an intermediate in preparing medicines, agricultural chemicals and other chemical products.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05600036 |
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| Source dataset | uspto-grants-1997_02 |
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| ORD ID | ord-8ff220c30c9640d8817eff80ec8162f2 |
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| Source note | uspto-grants-1997_02 |
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