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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 403505Generated: November 2, 2026

Diethyl Ether → (s)-2-Methyl-1-((s)-1-phenylethyl)piperidin-4-one

https://huagongshe.com/reaction/403505

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDiethyl EtherHCID 3283—
Reactant1-Phenethylamine, (-)-HCID 75818—
Reactant4-((2-Ethyl-5,7-dimethylpyrazolo[1,5-a]pyrimidin-3-yl)methyl)phenolHCID 68379224—
ReactantHCID 178418507HCID 178418507—
SolventWaterHCID 962—
SolventTetrahydrofuranHCID 8028—
Product(s)-2-Methyl-1-((s)-1-phenylethyl)piperidin-4-oneHCID 13198301—

Reaction Steps

In a flame dried roundbottomflask (E)-but-2-enoic acid methoxy-methyl-amide (Einhorn et al., Synth. Commun. 20 (8), 1105-1112 (1990)) (8.0 g, 61.9 mmol) was dissolved in 150 ml of THF. A 1M solution of vinylmagnesium bromide in Et2O (68.1 ml, 68.1 mmol) was added at 0° C. and then the mixture was stirred for 1 h at rt. (S)-(−)-alpha-methylbenzylamin (15.8 ml, 124 mmol) was added at rt, followed by water (15 ml). The reaction was stirred at rt for 1 h. THF was evaporated and 150 ml of water was added. Then the mixture was extracted three times with CH2Cl2 The organic layer was washed with brine, dried over Na2 SO4 and evaporated. The crude product was purified by flash chromatography (silica gel, 20% EtOAc/cyclohexane) which furnished the (S,S) product as the first fraction (confirmed by x-ray).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08748435B2
Source datasetuspto-grants-2014_06
ORD IDord-a6168759d9774d9e921ad1fdd8afc9d1
Source noteuspto-grants-2014_06