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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2382191Generated: October 30, 2026

tert-Butyl 4-(methoxy(methyl)carbamoyl)piperidine-1-carboxylate → Tert-butyl 4-benzoylpiperidine-1-carboxylate

https://huagongshe.com/reaction/2382191

Reaction equation

Participants

RoleNameHCIDCharge
Reactanttert-Butyl 4-(methoxy(methyl)carbamoyl)piperidine-1-carboxylateHCID 11065582—
ReactantHCID 178478979HCID 178478979—
SolventTetrahydrofuranHCID 8028—
ProductTert-butyl 4-benzoylpiperidine-1-carboxylateHCID 1082730759%

Reaction Steps

To a solution of tert-butyl 4-(methoxy(methyl)carbamoyl)piperidine-1-carboxylate (8.0 g, 29.4 mmol) in THF (25 mL) was added PhMgCl (8.0 g, 58.8 mmol) dropwise at 0° C. After stirring at rt for 2 h, the reaction was quenched with ammonium chloride solution and extracted with ethyl acetate, dried over anhydrous sodium sulfate and concentrated under vacuum to afford tert-butyl 4-benzoylpiperidine-1-carboxylate (5 g, 59% yield) as a pale yellow solid which was used directly in the next step.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08258306B2
Source datasetuspto-grants-2012_09
ORD IDord-5aa05b7ef335495ab0f1d54e49721986
Source noteuspto-grants-2012_09