HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2379277Generated: October 26, 2026
Acetyl chloride → N-[3-(trifluoromethyl)phenyl]-N-propargyl-N'-acetylthiourea
https://huagongshe.com/reaction/2379277
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Acetyl chloride | HCID 6367 | — |
| Reactant | Potassium thiocyanate | HCID 516872 | — |
| Reactant | Benzenamine, N-2-propyn-1-yl-3-(trifluoromethyl)- | HCID 10488213 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | N-[3-(trifluoromethyl)phenyl]-N-propargyl-N'-acetylthiourea | HCID 11120113 | — |
Reaction Steps
Acetyl chloride (2.75 g) is mixed with acetonitrile (70 ml), and the mixture is cooled to 0° C. Then, potassium thiocyanate (3.75 g) is added thereto, and the mixture is stirred at room temperature for 6 hours. After cooling to 0° C. again, 3-trifluoromethyl-N-propargylaniline (7 g) is added thereto, and the mixture is stirred at room temperature for 3 hours. After the solvent is distilled off under reduced pressure, the residue is extracted with ethyl acetate (300 ml), and the extract is washed with water. The solvent is distilled off to give N-[3-(trifluoromethyl)phenyl]-N-propargyl-N'-acetylthiourea as crystallines (8 g). This identification is achieved by proton nuclear magnetic resonance (1H-NMR ).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05360912 |
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| Source dataset | uspto-grants-1994_11 |
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| ORD ID | ord-7cd1eaaee2054133a0cbc33c57a65b64 |
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| Source note | uspto-grants-1994_11 |
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