Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | 3-Chloro-4-fluoro-5-nitrobenzotrifluoride | HCID 2736565 | — |
| Solvent | Hydrochloric Acid | HCID 313 | — |
| Product | HCID 19779367 | HCID 19779367 | 73% |
Reaction Steps
5-Chloro-4-fluoro-3-nitrotrifluoromethylbenzene (50 g) was added to a cooled (5° C.) solution of stannous chloride (140 g) in concentrated aqueous hydrochloric acid (187 ml). After stirring for several hours at the ambient temperature (about 22° C.), the reaction mixture was stood overnight. After basification by the addition of sodium hydroxide, the reaction mixture was extracted with ethyl acetate. The organic layer was washed with water, dried, and the solvent removed by evaporation under reduced pressure. The residual yellow oil was kugelrohr distilled under reduced pressure to give 3-amino-5-chloro-4-fluorotrifluoromethylbenzene (32 g): boiling point 105° C./11 mm Hg;
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05079251 |
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| Source dataset | uspto-grants-1992_01 |
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| ORD ID | ord-f3d614fe38504ec09e464a0dd01f94bc |
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| Source note | uspto-grants-1992_01 |
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