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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 403506Generated: November 1, 2026

tert-butyl (2S)-2-methyl-4-oxopiperidine-1-carboxylate → (2S)-Tert-butyl 4-allyl-4-hydroxy-2-methylpiperidine-1-carboxylate

https://huagongshe.com/reaction/403506

Reaction equation

Participants

RoleNameHCIDCharge
Reactanttert-butyl (2S)-2-methyl-4-oxopiperidine-1-carboxylateHCID 11401606—
ReactantHCID 178455850HCID 178455850—
SolventDiethyl EtherHCID 3283—
Product(2S)-Tert-butyl 4-allyl-4-hydroxy-2-methylpiperidine-1-carboxylateHCID 68379051—

Reaction Conditions

Temperature0 °C

Reaction Steps

In a argon flushed dry 25 ml 2-neckoundbottomflask (S)-2-methyl-4-oxo-piperidine-1-carboxylic acid tert-butyl ester (34) (0.6 g, 2.81 mmol) was dissolved in 10 ml of ether. A 1M solution of allylmagnesiumbromide in Et2O (3.66 ml, 3.66 mmol) was added dropwise at 0° C. The reaction mixture was stirred at 0° C. for 2 h. The mixture was quenched with NH4Cl solution and extracted with ether. The organic layer was washed with brine, dried over Na2 SO4 and evaporated. The crude product was purified by flash chromatography (silica gel, 20-30% EtOAc/cyclohexane) which furnished the product as white solid

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08748435B2
Source datasetuspto-grants-2014_06
ORD IDord-821fde4c95414ddb8f3cf416e7d0b7fa
Source noteuspto-grants-2014_06