HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1989065Generated: November 1, 2026
Trifluoroacetic acid → HCID 68678854, compound
https://huagongshe.com/reaction/1989065
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Trifluoroacetic acid | HCID 6422 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | 2-(Dimethylamino)acetyl chloride | HCID 7010344 | — |
| Reactant | tert-Butyl [3-(piperidin-4-yl)phenyl]carbamate | HCID 29948324 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 68678854 | HCID 68678854 | 48% |
Reaction Steps
Dimethylamino-acetyl chloride (0.14 g, 0.86 mmol) and (3-piperidin-4-yl-phenyl)-carbamic acid tert-butyl ester (0.20 g, 0.72 mmol) were combined in CH2Cl2 (5 mL) and triethylamine (0.21 g, 2.2 mmol) was added. After 6 h, water (5 mL) was added. The reaction mixture was extracted with CH2Cl2 (3×5 mL) and the combined organic extracts were dried (MgSO4) and concentrated. The compound was found to be unstable on silica and therefore carried on without further purification. (3-Piperidin-4-yl-phenyl)-carbamic acid tert-butyl ester (0.72 mmol) was diluted in CH2Cl2 (3 mL) and TFA (3 mL) was added. After 1 h, the reaction mixture was concentrated. Water (2 mL) was added and the solution was frozen and lyophilized overnight to provide (0.090 g) (48%) of 1-[4-(3-amino-phenyl)-piperidin-1-yl]-2-dimethylamino-ethanone.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07642270B2 |
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| Source dataset | uspto-grants-2010_01 |
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| ORD ID | ord-19f430d55ed9473c9c5fb5ebac4e4645 |
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| Source note | uspto-grants-2010_01 |
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