HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1850693Generated: October 29, 2026
Trichloroacetonitrile → 3-amino-4,4,4-trichloro-2-cyano-N-(2-methyl-3-phenyl-imidazol-4-yl)but-2-enamide
https://huagongshe.com/reaction/1850693
Participants
| Role | Name | HCID | Charge |
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| Reactant | Trichloroacetonitrile | HCID 11011 | — |
| Reactant | Sodium Acetate | HCID 517045 | — |
| Reactant | 2-cyano-N-(2-methyl-3-phenyl-imidazol-4-yl)acetamide | HCID 90411763 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | 3-amino-4,4,4-trichloro-2-cyano-N-(2-methyl-3-phenyl-imidazol-4-yl)but-2-enamide | HCID 131732452 | — |
Reaction Steps
To a solution of 2-cyano-N-(2-methyl-3-phenyl-imidazol-4-yl)acetamide (100 mg, 0.4162 mmol) in Ethanol (1.5 mL) was sequentially added sodium acetate (68.28 mg, 0.8324 mmol), 2,2,2-trichloroacetonitrile (0.051 mL, 0.5016 mmol) and the reaction was stirred at room temperature for 4 h. A further 10 mg of sodium acetate and 10 uL 2,2,2-trichloroacetonitrile was sequentially added and the mixture was stirred for a further 2 h at RT. The reaction was concentrated in vacuo and the residue was partitioned between water and EtOAc. Combined organic extract was washed with brine, dried (MgSO4) and concentrated in vacuo to give 3-amino-4,4,4-trichloro-2-cyano-N-(2-methyl-1-phenyl-1H-imidazol-5-yl)but-2-enamide as a redish oil. (153 mg, 79%). MS (ES+) 384.0.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08957078B2 |
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| Source dataset | uspto-grants-2015_02 |
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| ORD ID | ord-af3f1adaec8847dbb4522a2ea583c986 |
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| Source note | uspto-grants-2015_02 |
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