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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1963312Generated: October 31, 2026

Triethylamine → HCID 66732104, compound

https://huagongshe.com/reaction/1963312

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
Reactanttert-Butyl methyl etherHCID 15413—
ReactantLithium BromideHCID 82050—
ReactantDimethyl 2-(2,5-difluorobenzyl)piperidine-1,4-dicarboxylateHCID 66734456—
SolventWaterHCID 962—
SolventAcetonitrileHCID 6342—
ProductHCID 66732104HCID 6673210496%

Reaction Steps

To a solution of dimethyl 2-(2,5-difluorobenzyl)piperidine-1,4-dicarboxylate (8.08 g, 24.69 mmol) in acetonitrile (85 mL) and water (1.7 mL) was added lithium bromide (4.95 mL, 197.48 mmol) and triethylamine (13.69 mL, 98.74 mmol). The reaction mixture was heated to reflux for 2.5 h, then allowed to cool to room temperature. Water (150 mL) and MTBE (300 mL) was added. The aqueous phase was separated and the organic phase was extracted twice with water. The water phases were combined and 4.0 M HCl was added until a pH of 1 was obtained. The aqueous was extracted with MTBE (300 mL×2). The organic phases were combined, washed with brine, dried with Na2SO4 and evaporated under reduced pressure to give 2-(2,5-difluorobenzyl)-1-(methoxycarbonyl)piperidine-4-carboxylic acid (7.4 g, 96%). MS m/z 314 (M+H)+

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08415378B2
Source datasetuspto-grants-2013_04
ORD IDord-646a8fb5c1cb4d8da110a5b14e4f6acc
Source noteuspto-grants-2013_04