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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1171748Generated: November 1, 2026

Sodium Chloride → 1,2,3,6-Tetrahydro-1-(triphenylmethyl)pyridine

https://huagongshe.com/reaction/1171748

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium ChlorideHCID 5234—
Reactant1,1-Bis(2,2-dimethylpropoxy)-N,N-dimethylmethanamineHCID 78623—
ReactantHCID 68766248HCID 68766248—
ReactantHCID 86609484HCID 86609484—
ReactantHCID 178418634HCID 178418634—
SolventTolueneHCID 1140—
Product1,2,3,6-Tetrahydro-1-(triphenylmethyl)pyridineHCID 186887170.4%

Reaction Steps

To a solution of (E)-3-{[1-(4-methoxybenzyl)-1H-1,2,3-triazol-4-yl]methylidene}-1-(triphenylmethyl)piperidin-4-ol (17.45 g) in toluene (300 ml) were added thioacetic acid (4.6 ml) and N,N-dimethylformamide dineopentylacetal (18 ml). The resulting solution was stirred at room temperature for 15 minutes, and the reaction was stopped by an addition of a saturated aqueous sodium chloride solution. The products were extracted with ethyl acetate, and the extract was dried over anhydrous sodium sulfate and concentrated in vacuo. The residue was purified by chromatography on silica gel using a mixture of hexane, ethyl acetate and dichloromethane (1:1:1) as the eluent to afford an approximately 1:3 mixture of (E)-4-(acetylsulfanyl)-3-{[1-(4-methoxybenzyl)-1H-1,2,3-triazol-4-yl]methylidene}-1-(triphenylmethyl)piperidine and 5-(acetylsulfanyl){[1-(4-methoxybenzyl)-1H-1,2,3-triazol-4-yl]methylidene}methyl)-1-(triphenylmethyl)-1,2,3,6-tetrahydropyridine (17.83 g, yield: 92%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07829580B2
Source datasetuspto-grants-2010_11
ORD IDord-ebcee231a52c4573ae858beb04532901
Source noteuspto-grants-2010_11