HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 37362Generated: October 29, 2026
Trifluoroacetic anhydride → Trifluoroacetic acid
https://huagongshe.com/reaction/37362
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Trifluoroacetic anhydride | HCID 9845 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | Trifluoroacetic acid | HCID 6422 | — |
| Product | Trifluoroacetic anhydride | HCID 9845 | — |
Reaction Steps
To 20 g of the compound of Example 20B suspended in 60 ml dichloromethane was added at -20° C. a solution of 100 ml trifluoroacetic acid anhydride in 40 ml dichloromethane. While stirring, an orange colored solution was obtained after 30 minutes. The solution was then stirred at 0° C. for one hour. The color turned to a dark green. The solvent, excess trifluoroacetic acidanhydride and formed trifluoroacetic acid was then distilled of in vacuo at room temperature. After evaporation with an oil-vacuo for additional one hour a beige foam was obtained. This was stirred with 150 ml ether and cooled to -20° C. A dark red suspension was obtained. After filtration and washing with ether and hexane the title compound was obtained as a beige solid (20.4 g). The compound is unstable and must be immediately used for further transformation.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05420277 |
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| Source dataset | uspto-grants-1995_05 |
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| ORD ID | ord-1a2c9956d39a416a8fb4300a11f40fa5 |
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| Source note | uspto-grants-1995_05 |
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