HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 975513Generated: October 29, 2026
Ammonia → [2,6-Dichloro-4-(trifluoromethyl)phenyl]hydrazine
https://huagongshe.com/reaction/975513
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Ammonia | HCID 222 | — |
| Reactant | Sodium Nitrite | HCID 23668193 | — |
| Reactant | 2,6-Dichloro-4-trifluoromethylphenylaniline | HCID 54490724 | — |
| Solvent | Acetic Acid | HCID 176 | — |
| Solvent | Hydrochloric Acid | HCID 313 | — |
| Solvent | Sulfuric Acid | HCID 1118 | — |
| Product | [2,6-Dichloro-4-(trifluoromethyl)phenyl]hydrazine | HCID 688223 | 107.5% |
Reaction Steps
2,6-Dichloro-4-trifluoromethylphenylaniline (4.3 g) was dissolved with stirring, in glacial acetic acid (23 ml). A solution of sodium nitrite (1.5 g) in concentrated sulphuric acid (11 ml) was then added at 55°-60° C. The solution thus obtained was cooled to 0°-5° C. and a solution of stannous chloride (16.4 g) in concentrated hydrochloric acid (14 ml) was added with vigorous stirring. A cream-colored solid precipitated. The mixture was filtered and the solid obtained was added to a mixture of aqueous ammonia solution and ice. The mixture thus obtained was extracted with diethyl ether (6×500 ml) and the combined ethereal extracts were dried over sodium sulphate, filtered and evaporated to dryness to give 2,6-dichloro-4-trifluoromethylphenylhydrazine (3.7 g) m.p. 54°-56° C., in the form of a colorless crystalline solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05608077 |
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| Source dataset | uspto-grants-1997_03 |
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| ORD ID | ord-1c840f4e63474997b89e3034f0c4d618 |
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| Source note | uspto-grants-1997_03 |
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