HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1983754Generated: October 29, 2026
Trifluoroacetic acid → HCID 22556557, compound
https://huagongshe.com/reaction/1983754
Participants
| Role | Name | HCID | Charge |
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| Reactant | Trifluoroacetic acid | HCID 6422 | — |
| Reactant | 1,1-Dimethylethyl 4-[[2-(4-chlorophenyl)acetyl]amino]-1-piperidinecarboxylate | HCID 47069170 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 22556557 | HCID 22556557 | — |
Reaction Steps
A solution of 4-[2-(4-chloro-phenyl)-acetylamino]-piperidine-1-carboxylic acid tert-butyl ester (0.55 g, 1.54 mmol) in dichloromethane (8.0 mL) cooled at 0° C. was treated with trifluoroacetic acid (20%) and warmed to room temperature and stirred for 2 h. The reaction mixture was concentrated in vacuo, diluted with ethyl acetate and free based with 10% aqueous sodium bicarbonate. The combined organic layers were dried over sodium sulfate and concentrated in vacuo. The crude product was purified on silica using gradient elution from ethyl acetate/methanol (2%) to ethyl acetate/methanol (20%). 1H-NMR (CDCL3) δ: 1.15-1.25 (2H, m), 1.80-1.90 (2H, m), 2.60-2.75 (2H, m), 2.90-3.10 (2H, m), 3.5 (2H, s), 3.85 (1H, m), 5.20 (1H, d), 7.15-7.35 (4H, m). ESI-MS m/z: 253 (M+1), UV retention time: 0.87 min.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07541365B2 |
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| Source dataset | uspto-grants-2009_06 |
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| ORD ID | ord-9ed2ab1c4d39463a98a77d81763acaf4 |
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| Source note | uspto-grants-2009_06 |
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