HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 57389Generated: October 30, 2026
Diisopropylethylamine → 3-Chloro-N'-hydroxy-4-(trifluoromethoxy)benzimidamide
https://huagongshe.com/reaction/57389
Participants
| Role | Name | HCID | Charge |
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| Reactant | Diisopropylethylamine | HCID 81531 | — |
| Reactant | Hydroxyamine hydrochloride | HCID 443297 | — |
| Reactant | 3-chloro-4-(trifluoromethoxy)benzonitrile | HCID 2773846 | — |
| Solvent | Ethanol | HCID 702 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | 3-Chloro-N'-hydroxy-4-(trifluoromethoxy)benzimidamide | HCID 58538786 | 62.1% |
Reaction Steps
To a solution of 3-chloro-4-(trifluoromethoxy)benzonitrile (1.0 g, 4.51 mmol) and hydroxylamine hydrochloride (1.5 eq, 0.47 g, 6.77 mmol) in ethanol (10 ml) was added N-ethyl-N-isopropylpropan-2-amine (1.6 eq, 1.26 ml, 7.22 mmol) and refluxed at 80° C. for 12 hours under N2. Allow to cool to rt. Dilute with EtOAc (25 ml), wash with water (25 ml), brine (25 ml), dry, concentrate in vacuo afforded (Z)-3-chloro-N′-hydroxy-4-(trifluoromethoxy)benzimidamide (0.71 g, 62.1%, white solid). Used crude in the next step. HRMS(B) m/z 254.0070
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09434719B2 |
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| Source dataset | uspto-grants-2016_09 |
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| ORD ID | ord-f649e413bff241dc97b169e89c7d8413 |
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| Source note | uspto-grants-2016_09 |
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