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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2165761Generated: October 26, 2026

Sodium Chloride → 1-Acetyl-4-hydroxy-4-(1-methyl-2-propenyl)piperidine

https://huagongshe.com/reaction/2165761

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium ChlorideHCID 5234—
ReactantCrotyl chlorideHCID 11589—
ReactantN-Acetyl-4-piperidoneHCID 122563—
ReactantMagnesiumHCID 5462224—
SolventDiethyl EtherHCID 3283—
SolventTetrahydrofuranHCID 8028—
Product1-Acetyl-4-hydroxy-4-(1-methyl-2-propenyl)piperidineHCID 14852045—

Reaction Steps

To a solution of 1.94 g 1-acetyl-4-piperidone in a mixture of ether (80 ml) and tetrahydrofuran (40 ml), was added dropwise at 10° C. or lower 275 ml of a 0.5M Grignard reagent prepared by the usual way from crotyl chloride and magnesium, and the resulting mixture was stirred overnight at room temperature. To the ice-cooled reaction mixture, was slowly added 100 ml of saturated aqueous solution of sodium chloride, and the layers were separated. The aqueous layer was extracted with chloroform, the two organic solutions were each concentrated, and the combined concentrate was subjected to silica gel column chromatography using, as eluent, a mixed solvent of ethyl acetate/n-hexane (1:1 by volume) containing 3% methanol, giving 16.9 g of 1-acetyl-4-hydroxy-4-(1-methyl-2-propenyl)piperidine as oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04940795
Source datasetuspto-grants-1990_07
ORD IDord-993f2c5111a94819ad11f54a9ab4885e
Source noteuspto-grants-1990_07