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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 434665Generated: October 30, 2026

Bromine → 3-Bromo-3-methylpiperidin-2-one

https://huagongshe.com/reaction/434665

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBromineHCID 24408—
ReactantPhosphorus pentachlorideHCID 24819—
Reactant3-Methylpiperidin-2-oneHCID 107169—
ReactantSodium BisulfiteHCID 23665763—
CatalystZincchlorideHCID 3007855—
SolventChloroformHCID 6212—
Product3-Bromo-3-methylpiperidin-2-oneHCID 1304104981%

Reaction Conditions

Temperature0 °C

Reaction Steps

A mixture of 5.15 g of 3-methyl-2-piperidone (Ber. 24 page 2445) and 50 ml of chloroform is chilled to about 0° C. Then there are added while stirring at 0°-5° C. 19 g of phosphorus pentachloride, followed by 0.2 g of anhydrous zinc chloride. The mixture is heated to about 15° C., treated dropwise with a solution of 2.5 ml of bromine in 5 ml of chloroform and then heated to 40° C. for 5 hours, while stirring. After cooling the mixture is poured on ice and treated with sodium hydrogensulfite until it is discolored. The layers are separated and the aqueous phase is extracted with chloroform. The combined chloroform layers are dried over magnesium sulfate and then the solvent is distilled off in vacuo. The semi-solid residue is recrystallized from acetone to give 3-bromo-3-methyl-2-piperidone melting at 107° to 109° C. in a yield of 81% of the theoretical.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04399145
Source datasetuspto-grants-1983_08
ORD IDord-ce93a624331f44489c3688764d8ece61
Source noteuspto-grants-1983_08