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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1963261Generated: October 28, 2026

Triethylamine → 2-(4-Fluorophenethyl)-1-(methoxycarbonyl)piperidine-4-carboxylic acid

https://huagongshe.com/reaction/1963261

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
ReactantLithium BromideHCID 82050—
ReactantDimethyl 2-(4-fluorophenethyl)piperidine-1,4-dicarboxylateHCID 86646603—
SolventWaterHCID 962—
SolventAcetonitrileHCID 6342—
Solventtert-Butyl methyl etherHCID 15413—
Product2-(4-Fluorophenethyl)-1-(methoxycarbonyl)piperidine-4-carboxylic acidHCID 66732483143.7%

Reaction Steps

Dimethyl 2-(4-fluorophenethyl)piperidine-1,4-dicarboxylate (3.18 g, 9.83 mmol) was dissolved in acetonitrile (35 mL) and water (0.7 mL) and lithium bromide (6.83 g, 78.67 mmol) was added. Triethylamine (5.45 mL, 39.34 mmol) was added and the resulting suspension was heated under reflux for 5 h. MTBE and water were added, the phases separated and the organic layer was extracted with water. The combined aqueous layers were acidified to pH 1 with 3.8 M HCl and extracted with MTBE. The combined organic layers were washed with water, dried with Na2SO4 and evaporated. Crude 2-(4-fluorophenethyl)-1-(methoxycarbonyl)piperidine-4-carboxylic acid (4.37 g) was isolated. MS m/z 310 (M+H)+

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08415378B2
Source datasetuspto-grants-2013_04
ORD IDord-3cad11dcf3e94f9a954b52bd743903db
Source noteuspto-grants-2013_04