HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1255390Generated: October 25, 2026
3,5-Dichlorosalicylaldehyde → 3-Trifluoromethoxy-benzoic acid [1-(3,5-dichloro-2-hydroxy-phenyl)-methylidene]-hydrazide
https://huagongshe.com/reaction/1255390
Participants
| Role | Name | HCID | Charge |
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| Reactant | 3,5-Dichlorosalicylaldehyde | HCID 66660 | — |
| Reactant | 3-(Trifluoromethoxy)benzohydrazide | HCID 3801099 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | 3-Trifluoromethoxy-benzoic acid [1-(3,5-dichloro-2-hydroxy-phenyl)-methylidene]-hydrazide | HCID 136359955 | 99.8% |
Reaction Steps
A suspension of 3,5-dichloro-2-hydroxy-benzaldehyde (0.200, 1.05 mmol) and 3-trifluoromethoxy-benzoic acid hydrazide (0.243 g, 1.05 mmol) in ethanol (3.3 mL) was heated to 60° C. for 18 hours. The reaction mixture was cooled to room temperature to precipitate the product. The solid was collected via suction filtration and rinsed with ethanol to furnish 3-trifluoromethoxy-benzoic acid [1-(3,5-dichloro-2-hydroxy-phenyl)-methylidene]-hydrazide as an off-white solid (0.412 g, 99%): mp 180-182° C.; 1H NMR (400 MHz, DMSO) δ 12.63 (s, 1H), 12.39 (s, 1H), 8.60 (s, 1H), 8.01 (d, J=7.6 Hz, 1H), 7.91 (s, 1H), 7.76-7.63 (m, 4H); ESIMS m/z 393 ([M+H]+), 391 ([M−H]−).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08461078B2 |
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| Source dataset | uspto-grants-2013_06 |
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| ORD ID | ord-f3126be4d8164dde9eb6a8eda61a8b66 |
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| Source note | uspto-grants-2013_06 |
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