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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1989065Generated: November 1, 2026

Trifluoroacetic acid → HCID 68678854, compound

https://huagongshe.com/reaction/1989065

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTrifluoroacetic acidHCID 6422—
ReactantTriethylamineHCID 8471—
Reactant2-(Dimethylamino)acetyl chlorideHCID 7010344—
Reactanttert-Butyl [3-(piperidin-4-yl)phenyl]carbamateHCID 29948324—
SolventWaterHCID 962—
SolventDichloromethaneHCID 6344—
ProductHCID 68678854HCID 6867885448%

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07642270B2
Source datasetuspto-grants-2010_01
ORD IDord-19f430d55ed9473c9c5fb5ebac4e4645
Source noteuspto-grants-2010_01