HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 587844Generated: October 30, 2026
Trifluoroacetic acid → HCID 86666628, compound
https://huagongshe.com/reaction/587844
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Trifluoroacetic acid | HCID 6422 | — |
| Reactant | HCID 86666629 | HCID 86666629 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 86666628 | HCID 86666628 | — |
Reaction Steps
Tert-butyl (5-{[2-ethyl-4-(1,1,1,2,3,3,3-heptafluoropropan-2-yl)-6-methylphenyl]-carbamoyl}-2,3-dihydro-1H-inden-1-yl)carbamate (1.3 g) was dissolved in methylene chloride (15 ml), trifluoroacetic acid (1.5 g) was added thereto and then stirred at room temperature for 3 hours. The solvent was distilled off under reduced pressure. Water and potassium carbonate were added to neutralize the residue and extracted twice with ethyl acetate. The organic phases were combined, washed with a saturated sodium bicarbonate aqueous solution and water sequentially, and then dried over anhydrous magnesium sulfate. The drying agent was removed by filtration, and the solvent was distilled off under reduced pressure to obtain 1-amino-N-[2-ethyl-4-(1,1,1,2,3,3,3-heptafluoropropan-2-yl)-6-methylphenyl]indane-5-carboxamide as a crude product (0.84 g). The crude product was used for the next step without further purification.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09227923B2 |
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| Source dataset | uspto-grants-2016_01 |
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| ORD ID | ord-263969c101b546c681c125e3bd74d966 |
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| Source note | uspto-grants-2016_01 |
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