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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 132854Generated: October 26, 2026

Sulfuric acid magnesium salt (1:1) → HCID 69220530, compound

https://huagongshe.com/reaction/132854

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSulfuric acid magnesium salt (1:1)HCID 24083—
ReactantPyrrolidineHCID 31268—
ReactantAmmonium AcetateHCID 517165—
Reactant4-Ethoxy-1,1,1-trifluoro-3-buten-2-oneHCID 2780395—
Reactant1-Tritylpiperidin-3-oneHCID 22707051—
SolventTetrahydrofuranHCID 8028—
ProductHCID 69220530HCID 69220530—

Reaction Steps

A mixture of N-trityl-3-piperidone (1.22 g, 3.6 mmol), magnesium sulfate (2.70 g) and pyrrolidine (0.36 mL, 4.3 mmol) in 10 mL of tetrahydrofuran was stirred at room temperature for 72 h. The reaction mixture was filtered, and the filtrate was concentrated under reduced pressure. The resultant crude enamine was dissolved in 13 mL of dry dioxane, cooled to approximately 10° C. and treated dropwise with 4-ethoxy-1,1,1-trifluoro-3-buten-2-one (0.61 mL, 4.3 mmol). The resultant orange solution was allowed to warm to room temperature overnight. Ammonium acetate (0.60 g) was added to the blood-red solution, and the mixture was heated at reflux for 2.5 h, cooled to room temperature and concentrated under reduced pressure. The residue was stirred with 100 mL of dry ether, filtered through a pad of Celite, and concentrated under reduced pressure. The resultant dark red gum was purified by flash chromatography (silica gel; 3% ethyl acetate/hexanes as eluant) to afford impure product. A portion (147 mg) of this material was further purified by preparative TLC (silica gel; 5% ethyl acetate/hexanes as eluant) to afford the title compound as a light yellow foam. LC/MS 365.2 (M+1).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07388019B2
Source datasetuspto-grants-2008_06
ORD IDord-391b868f09bc46a1b71240b48f06877a
Source noteuspto-grants-2008_06