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
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Sodium Chloride | HCID 5234 | — |
| Reactant | 1,1-Bis(2,2-dimethylpropoxy)-N,N-dimethylmethanamine | HCID 78623 | — |
| Reactant | HCID 68766248 | HCID 68766248 | — |
| Reactant | HCID 86609484 | HCID 86609484 | — |
| Reactant | HCID 178418634 | HCID 178418634 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | 1,2,3,6-Tetrahydro-1-(triphenylmethyl)pyridine | HCID 186887 | 170.4% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07829580B2 |
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| Source dataset | uspto-grants-2010_11 |
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| ORD ID | ord-ebcee231a52c4573ae858beb04532901 |
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| Source note | uspto-grants-2010_11 |
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