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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 654129Generated: October 29, 2026

Diethyl Ether → Benzyl 3-methyl-4-oxopiperidine-1-carboxylate

https://huagongshe.com/reaction/654129

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDiethyl EtherHCID 3283—
ReactantBenzyl chloroformateHCID 10387—
ReactantSodium BicarbonateHCID 516892—
Reactant3-Methylpiperidin-4-one hydrobromideHCID 20094587—
SolventWaterHCID 962—
ProductBenzyl 3-methyl-4-oxopiperidine-1-carboxylateHCID 15233096—

Reaction Steps

To a mechanically stirred mixture of benzylchloroformate (33.1 mL, 232 mmol, 105 mol %), sodium bicarbonate (37.2 g, 442 mmol, 200 mol %), ether (250 mL), and water (250 mL) is added 3-methyl-4-piperidone hydrobromide salt (42.9 g, 221 mmol) in portions over 10 min. The resultant mixture is stirred for 2 h and the organic phase separated. The aqueous phase is extracted with ether (2×150 mL) and the combined organics dried (MgSO4), filtered, and concentrated to an oily residue. This residue crystallized on standing at 23° C. and was recrystallized from hexanes/ethyl acetate to give N-benzyloxycarbonyl-3-methyl-4-piperidone as a solid: 51.2 g; 93%; mp 33°-35° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05130321
Source datasetuspto-grants-1992_07
ORD IDord-b217e9c4e5ec4ac482ce11b78b7296c4
Source noteuspto-grants-1992_07