HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 628779Generated: October 29, 2026
Toluene → Ethyl 4-(2-(4-tolylsulfanyl)phenyl)-piperidin-1-carboxylate
https://huagongshe.com/reaction/628779
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Toluene | HCID 1140 | — |
| Reactant | Trifluoroacetic acid | HCID 6422 | — |
| Reactant | Triethylsilane | HCID 12052 | — |
| Reactant | 1-Carbethoxy-4-hydroxy-4-[2-(4-methylphenylsulfanyl)phenyl]piperidine | HCID 45258308 | — |
| Solvent | Water | HCID 962 | — |
| Product | Ethyl 4-(2-(4-tolylsulfanyl)phenyl)-piperidin-1-carboxylate | HCID 45258309 | — |
Reaction Steps
Trifluoroacetic acid (2.8 kg, 24.9 mol) and triethylsilane (362 g, 3.1 mol) was charged in a reactor with an efficient stirrer. Ethyl 4-hydroxy-4-(2-(4-tolylsulfanyl)phenyl)-piperidin-1-carboxylate (462 g, 1.24 mol) was added via a powder funnel in portions. The reaction was slightly exothermic. The temperature rose to 50° C. After the addition was finalised the reaction mixture was warmed to 60° C. for 18 hours. The reaction mixture was cooled down to room temperature. Toluene (750 mL) and water (750 mL) was added. The organic phase was isolated and the aqueous phase was extracted with another portion of toluene (750 mL). The organic phases were combined and washed with sodium chloride solution (15%, 500 mL) and dried over sodium sulphate. The sodium sulphate was filtered off, the filtrate evaporated at reduced pressure to a red oil which was processed further in the next step.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09315459B2 |
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| Source dataset | uspto-grants-2016_04 |
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| ORD ID | ord-e9ffdf15c91c4643baa1f7dcbafe5300 |
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| Source note | uspto-grants-2016_04 |
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