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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1986944Generated: October 31, 2026

Hydrochloric Acid → 4-(7-Trifluoromethyl-benzo[b]thiophen-3-yl)-piperidine

https://huagongshe.com/reaction/1986944

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantPotassium CarbonateHCID 11430—
Reactant1-[4-(7-Trifluoromethyl-benzo[b]thiophen-3-yl)-piperidin-1-yl]-ethanoneHCID 23112505—
SolventEthanolHCID 702—
Product4-(7-Trifluoromethyl-benzo[b]thiophen-3-yl)-piperidineHCID 1795213394.1%

Reaction Conditions

Temperature80 °C

Reaction Steps

A mixture of 1-[4-(7-trifluoromethyl-benzo[b]thiophen-3-yl)-piperidin-1-yl]-ethanone (2.95 g, 9.01 mmol), concentrated HCl (30 mL), and ethanol was heated at 80° C. for 18 h. After cooling to room temperature, the reaction was basified with 20% aqueous potassium carbonate (150 mL) and the mixture extracted with DCM (2×100 mL). The organics were washed with water (100 mL), dried over potassium carbonate, filtered, and concentrated to give 2.42 g (94%) the desired product as an amber waxy solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07550469B2
Source datasetuspto-grants-2009_06
ORD IDord-3612c57d38ee4cf687bf4f8931a8f78b
Source noteuspto-grants-2009_06