HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1694940Generated: November 1, 2026
Trifluoroacetic acid → HCID 66645881, compound
https://huagongshe.com/reaction/1694940
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Trifluoroacetic acid | HCID 6422 | — |
| Reactant | HCID 66645797 | HCID 66645797 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 66645881 | HCID 66645881 | 102.9% |
Reaction Steps
2.8 ml of trifluoroacetic acid (37 mmol) was added to a solution of 1.25 g of 2,2-dimethyl-4-(3-fluoro-2-methylphenyl)-5-oxopiperazine-1-carboxylic acid t-butyl ester obtained in Example (67c) (3.7 mmol) in methylene chloride (5.6 ml) at room temperature, and the mixture was stirred at the same temperature for 30 minutes. The reaction mixture was concentrated under reduced pressure. A saturated sodium bicarbonate aqueous solution was added, followed by extraction with methylene chloride. Then, the organic layer was dried over anhydrous magnesium sulfate. After filtration, the solvent was evaporated under reduced pressure, and the residue was purified by silica gel column chromatography (elution solvent:methylene chloride/methanol=10/1) to obtain 0.9 g of the title compound (yield: quant.).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08158790B2 |
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| Source dataset | uspto-grants-2012_04 |
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| ORD ID | ord-fce9faa7a6d8467caedf6a1447279fd4 |
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| Source note | uspto-grants-2012_04 |
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