HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 518933Generated: October 30, 2026
Trifluoroacetic acid → HCID 131733365, compound
https://huagongshe.com/reaction/518933
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Trifluoroacetic acid | HCID 6422 | — |
| Reactant | Triphenylphosphine | HCID 11776 | — |
| Reactant | Di-tert-butyl azodicarboxylate | HCID 97268 | — |
| Reactant | 2-Hydroxy-1-(piperidin-1-yl)ethan-1-one | HCID 6480489 | — |
| Reactant | HCID 131733364 | HCID 131733364 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | HCID 131733365 | HCID 131733365 | — |
Reaction Steps
The compound of Step D (3.0 g, 2.9 mmol) is dissolved in 100 mL of toluene. 1.53 g (5.8 mmol) of triphenylphosphine and 0.62 g (4.3 mmol) of 2-hydroxy-1-(1-piperidyl)ethanone are added thereto. The mixture is heated to 50° C., and then 1.01 g (4.3 mmol) of di-tert-butyl azodicarboxylate are added. The reaction mixture is stirred at 50° C. for 1 hour and is then allowed to return to ambient temperature before adding 1 mL of trifluoroacetic acid. After stirring overnight at ambient temperature, the mixture is successively washed with water, saturated NaHCO3 and brine solution. The combined aqueous phases are extracted with ethyl acetate. The resulting organic phases are dried over sodium sulphate, filtered and concentrated under reduced pressure. The crude product obtained is purified by chromatography over silica gel (dichloromethane/ethanol 98/2) to yield the expected compound.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09115159B2 |
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| Source dataset | uspto-grants-2015_08 |
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| ORD ID | ord-346dae02969e4883a7aab675b3feca46 |
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| Source note | uspto-grants-2015_08 |
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