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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1171725Generated: November 3, 2026

1,1-Bis(2,2-dimethylpropoxy)-N,N-dimethylmethanamine → HCID 23139094, compound

https://huagongshe.com/reaction/1171725

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1,1-Bis(2,2-dimethylpropoxy)-N,N-dimethylmethanamineHCID 78623—
ReactantHCID 23139200HCID 23139200—
ReactantHCID 178418634HCID 178418634—
SolventTolueneHCID 1140—
ProductHCID 23139094HCID 2313909478%

Reaction Steps

To a solution of (E)-3-{[1-(ethoxycarbonylmethyl)-1H-imidazol-2-yl]methylidene}-1-(triphenylmethyl)piperidin-4-ol (4.52 g) in toluene (80 ml) were added N,N-dimethylformamide dineopentyl acetal (5.0 ml) and thioacetic acid (1.3 ml) at 0° C. After the mixture was stirred at room temperature, the reaction was quenched by addition of water. The product was extracted with ethyl acetate. The organic layer was washed with a saturated aqueous sodium chloride solution and dried over anhydrous sodium sulfate. Removal of the solvent under reduced pressure followed by purification of the residue by silica gel chromatography using ethyl acetate and hexane (25:75 to 70:30) gave 5-{(acetylsulfanyl)[1-(ethoxycarbonylmethyl)-1H-imidazol-2-yl]methyl}-1-(triphenylmethyl)-1,2,3,6-tetrahydropyridine (3.92 g, yield: 78%) as a pale yellow amorphous solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07829580B2
Source datasetuspto-grants-2010_11
ORD IDord-3be28ddf5fe943e999fb6c2198dad625
Source noteuspto-grants-2010_11