HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1799009Generated: October 30, 2026
Trifluoroacetic acid → HCID 46191561, compound
https://huagongshe.com/reaction/1799009
Participants
| Role | Name | HCID | Charge |
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| Reactant | Trifluoroacetic acid | HCID 6422 | — |
| Reactant | HCID 59492764 | HCID 59492764 | — |
| Solvent | 1,4-Dioxane | HCID 31275 | — |
| Product | HCID 46191561 | HCID 46191561 | 96% |
Reaction Steps
To a mixture of 1,4-dioxane (6.7 ml) and an optically active form (1.34 g) of t-butyl 3-[4-(9-hydroxy-2-methyl-9-trifluoromethyl-9H-fluoren-4-yl)-pyrazol-1-yl]-propionate was added trifluoroacetic acid (6.7 ml), and the mixture was stirred at room temperature for 4 hr. The reaction mixture was concentrated under reduced pressure. Toluene was added to the obtained residue and the mixture was concentrated under reduced pressure. To the residue was added water (10 ml) and the mixture was extracted twice with ethyl acetate (10 ml). The combined organic layer was washed twice with water (10 ml) and once with saturated brine (10 ml), and dried over anhydrous sodium sulfate. Insoluble material was filtered off, and the obtained filtrate was concentrated under reduced pressure. Toluene was added to the obtained residue and the mixture was concentrated under reduced pressure. n-Hexane (10 ml) was added to the concentrated residue, and the slurry was stirred and filtered. The obtained solid was washed with n-hexane, and dried under reduced pressure to give the title compound (1.12 g, 96%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08343994B2 |
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| Source dataset | uspto-grants-2013_01 |
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| ORD ID | ord-d5fe29970f564dbd8d68eeee1a6e1368 |
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| Source note | uspto-grants-2013_01 |
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