Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1787890Generated: October 30, 2026

Pyrrolidine → Methyl 2-(1-tert-Butoxycarbonylpiperidin-4-yloxy)-4-(pyrrolidin-1-yl)benzoate

https://huagongshe.com/reaction/1787890

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPyrrolidineHCID 31268—
ReactantMethyl 2-(1-tert-Butoxycarbonylpiperidin-4-yloxy)-4-fluorobenzoateHCID 57602502—
ProductMethyl 2-(1-tert-Butoxycarbonylpiperidin-4-yloxy)-4-(pyrrolidin-1-yl)benzoateHCID 57602510282.8%

Reaction Conditions

Temperature80 °C

Reaction Steps

The methyl 2-(1-tert-butoxycarbonylpiperidin-4-yloxy)-4-fluorobenzoate (7.99 mmol, 22.6 mmol) was diluted with pyrrolidine (18 mL, 215.6 mmol). The resulting mixture was heated to 80° C. After 3 h, the reaction mixture was cooled to room temperature and quenched with water (50 mL). The mixture was extracted with dichloromethane (200 mL). The organic layer was washed with saturated aqueous citric acid (3×50 mL), dried over sodium sulfate, filtered, and concentrated to give the title compound (9.14 g, 100%) as a colorless oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07511066B2
Source datasetuspto-grants-2009_03
ORD IDord-474ff65ba61c420db473efdf7d92bd68
Source noteuspto-grants-2009_03