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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1963132Generated: October 30, 2026

Lithium Bromide → 2-(3,4-Difluorophenyl)-1-(methoxycarbonyl)piperidine-4-carboxylic acid

https://huagongshe.com/reaction/1963132

Reaction equation

Participants

RoleNameHCIDCharge
ReactantLithium BromideHCID 82050—
ReactantDimethyl 2-(3,4-difluorophenyl)piperidine-1,4-dicarboxylateHCID 66734537—
SolventWaterHCID 962—
SolventTetrahydrofuranHCID 8028—
Product2-(3,4-Difluorophenyl)-1-(methoxycarbonyl)piperidine-4-carboxylic acidHCID 6673155590.1%

Reaction Conditions

Temperature80 °C

Reaction Steps

Dimethyl 2-(3,4-difluorophenyl)piperidine-1,4-dicarboxylate (6.578 g, 21.00 mmol) was dissolved in THF (40 mL) and water (0.800 mL). Lithium bromide (14.59 g, 167.97 mmol) and TEA (11.71 mL, 83.98 mmol) were added and the reaction was stirred at 80° C. for 3 h. The reaction mixture was cooled to room temperature and some solvent evaporated in vacuo. EtOAc (150 mL) and water (150 mL) were added, shaken and the phases separated. The organic phase was extracted with water (150 mL). The combined aqueous phases were acidified with 3 M HCl to pH 1 and extracted with EtOAc (2×300 mL). The combined organic phases were dried with Na2SO4, filtered and evaporated in vacuo to yield 2-(3,4-difluorophenyl)-1-(methoxycarbonyl)piperidine-4-carboxylic acid (5.66 g, 90%) as a light brown oil. MS m/z 298 (M+H)+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08415378B2
Source datasetuspto-grants-2013_04
ORD IDord-ff96c9fb2dbb4ef68464ee356d548ee0
Source noteuspto-grants-2013_04