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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1963207Generated: October 29, 2026

Triethylamine → HCID 66731660, compound

https://huagongshe.com/reaction/1963207

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
Reactanttert-Butyl methyl etherHCID 15413—
ReactantLithium BromideHCID 82050—
ReactantHCID 66734743HCID 66734743—
SolventWaterHCID 962—
SolventAcetonitrileHCID 6342—
ProductHCID 66731660HCID 6673166091.2%

Reaction Steps

Dimethyl 2-(4-chloro-3,5-difluorophenyl)piperidine-1,4-dicarboxylate (1.83 g, 5.26 mmol) was dissolved in acetonitrile (30 mL) and water (0.600 mL), then lithium bromide (3.66 g, 42.10 mmol) was added. Triethylamine (2.92 mL, 21.05 mmol) was added and the resulting suspension was heated under reflux for 4 h. MTBE (100 mL) and water (50 mL) 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 dried over Na2SO4 and evaporated to yield 2-(4-chloro-3,5-difluoro-phenyl)-1-(methoxycarbonyl)piperidine-4-carboxylic acid (1.600 g, 91%) as a light yellow solid. MS m/z 332 (M−H)−

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08415378B2
Source datasetuspto-grants-2013_04
ORD IDord-445f5e561cbe40b2a0c9b4a1a41fdac5
Source noteuspto-grants-2013_04