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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1963273Generated: October 28, 2026

Triethylamine → 2-(3-Fluorobenzyl)-1-(methoxycarbonyl)piperidine-4-carboxylic acid

https://huagongshe.com/reaction/1963273

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
Reactanttert-Butyl methyl etherHCID 15413—
ReactantLithium BromideHCID 82050—
ReactantDimethyl 2-(3-fluorobenzyl)piperidine-1,4-dicarboxylateHCID 66734612—
SolventWaterHCID 962—
SolventAcetonitrileHCID 6342—
Product2-(3-Fluorobenzyl)-1-(methoxycarbonyl)piperidine-4-carboxylic acidHCID 6673250781%

Reaction Steps

Dimethyl 2-(3-fluorobenzyl)piperidine-1,4-dicarboxylate (9.153 g, 29.59 mmol) was dissolved in acetonitrile (100 mL) and water (2 mL), then lithium bromide (20.56 g, 236.72 mmol) was added. Triethylamine (16.41 mL, 118.36 mmol) was added and the resulting brown suspension was heated at reflux for 2 h. Water (100 mL) and MTBE (300 mL) were added. The organic phase was extracted with water (×2). The pooled aqueous layer was acidified to pH 1 with 3.8 M HCl and then extracted with MTBE (×2). The combined organic layer was washed with water, dried over Na2SO4, filtered through a Celite containing filter and evaporated. 2-(3-Fluorobenzyl)-1-(methoxycarbonyl)piperidine-4-carboxylic acid (7.07 g, 81%) was isolated as a yellow solid. MS m/z 296 (M+H)+

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08415378B2
Source datasetuspto-grants-2013_04
ORD IDord-17934ee07343465689d70a196658a3d5
Source noteuspto-grants-2013_04