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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 42561Generated: October 27, 2026

Water → Methyl 1-benzylpiperidine-4-carboxylate

https://huagongshe.com/reaction/42561

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantBenzyl BromideHCID 7498—
ReactantTriethylamineHCID 8471—
ReactantMethyl isonipecotateHCID 424914—
SolventChloroformHCID 6212—
ProductMethyl 1-benzylpiperidine-4-carboxylateHCID 11436222924.2%

Reaction Steps

To a solution of methyl piperidine-4-carboxylate (10.00 g, 6.4 mmol) and triethylamine (10.32 g, 10.2 mmol) in CHCl3 (100 mL), benzyl bromide (14.69 g, 8.6 mmol) was added under argon atmosphere while cooling with a water and ice bath. The mixture was stirred at room temperature overnight. CHCl3 and water were added and the two phases were separated. The aqueous phase was extracted with CHCl3. The organic phase was dried over Na2SO4 and concentrated to dryness, to afford 13.80 g of the desired compound as an orange solid (yield: 88%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08536194B2
Source datasetuspto-grants-2013_09
ORD IDord-613a553cbe3646d580f88062a12ccac2
Source noteuspto-grants-2013_09