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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 530924Generated: October 31, 2026

Water → Tert-butyl 1-[2-(benzyloxy)-2-oxoethyl]piperidine-4-carboxylate

https://huagongshe.com/reaction/530924

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantBenzyl bromoacetateHCID 62576—
ReactantDiisopropylethylamineHCID 81531—
ReactantTert-butyl Piperidine-4-carboxylateHCID 1512676—
SolventAcetonitrileHCID 6342—
ProductTert-butyl 1-[2-(benzyloxy)-2-oxoethyl]piperidine-4-carboxylateHCID 66588152—

Reaction Steps

To a suspension (39 mL) of tert-butyl piperidine-4-carboxylate (2.6 g) in acetonitrile was added diisopropylethylamine (4.4 mL), subsequently, benzyl bromoacetate (2.0 mL) was added at room temperature in portions, and the mixture was stirred for 4 hours. To the reaction mixture was added water, followed by extraction with ethyl acetate. This was washed with an aqueous saturated sodium chloride solution, dried with anhydrous sodium sulfate, and concentrated. The residue was purified by silica gel column chromatography (hexane:ethyl acetate=1:3→0:1) to obtain the title compound (3.4 g) having the following physical property values.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09353113B2
Source datasetuspto-grants-2016_05
ORD IDord-2dc5b63d8e8140c19d7334c26d7ac4b1
Source noteuspto-grants-2016_05