HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1503099Generated: October 30, 2026
Carbon Tetrachloride → 2,2,2-Trifluoro-N-(4-methoxyphenyl)acetimidoyl Chloride
https://huagongshe.com/reaction/1503099
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Carbon Tetrachloride | HCID 5943 | — |
| Reactant | Trifluoroacetic acid | HCID 6422 | — |
| Reactant | P-Anisidine | HCID 7732 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Triphenylphosphine | HCID 11776 | — |
| Product | 2,2,2-Trifluoro-N-(4-methoxyphenyl)acetimidoyl Chloride | HCID 10421682 | — |
Reaction Steps
In a typical reaction, a mixture of about 3 equivalents of triphenylphosphine and trifluoroacetic acid in carbon tetrachloride is cooled to about 0° C. in an ice bath and a 20% excess of triethylamine is added. With continued cooling, about a 20% excess of p-methoxyaniline in carbon tetrachloride is slowly added. After completion of the addition, the mixture is heated to about 70° C. for several hours. After cooling, the reaction mixture is extracted with hexane and the solvent evaporated to provide crude 2,2,2-trifluoro-N-(4-methoxyphenyl)acetimidoyl chloride.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09212141B2 |
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| Source dataset | uspto-grants-2015_12 |
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| ORD ID | ord-bb89b0cf70c54064b0bc199ef52c8182 |
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| Source note | uspto-grants-2015_12 |
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