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
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | tert-butyl (2S)-2-methyl-4-oxopiperidine-1-carboxylate | HCID 11401606 | — |
| Reactant | HCID 178455850 | HCID 178455850 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Product | (2S)-Tert-butyl 4-allyl-4-hydroxy-2-methylpiperidine-1-carboxylate | HCID 68379051 | — |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08748435B2 |
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| Source dataset | uspto-grants-2014_06 |
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| ORD ID | ord-821fde4c95414ddb8f3cf416e7d0b7fa |
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| Source note | uspto-grants-2014_06 |
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