Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Toluene-p-sulphonic anhydride | HCID 77773 | — |
| Reactant | 4-Piperidineethanol, 1-benzoyl- | HCID 10421498 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | HCID 15229595 | HCID 15229595 | 89% |
Reaction Steps
A solution of p-toluene sulfonic anhydride (6.0 g, 18 mmol) in dichloromethane (50 mL) was added dropwise over 1 hour to a room temperature solution of 1-benzoyl-4-hydroxyethylpiperidine (4.3 g, 18 mmol) and dry triethylamine (2.8 mL, 2 mmol) in dichloromethane. After 2 hours, the mixture was diluted with ethyl acetate (500 mL) and extracted successively with H2O (2 ×100 mL), cold 0.1 M aqueous HCl (100 mL), saturated aqueous NaHCO3 (100 mL), and brine (50 mL), dried (MgSO4), filtered, and concentrated in vacuo. The crude product was purified by chromatography on silica gel, eluting with ethyl acetate, and concentrated to yield a crystalline solid (6.2 g, 89%) which melted at 81°-83° C. Analysis: Calculated for C21H25NO4S: C,65.09; H,6.50; N,3.61; S,8.27; found: C.,65.31; H,6.74; N,3.41; S,8.30.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05317024 |
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| Source dataset | uspto-grants-1994_05 |
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| ORD ID | ord-876f9b564e044606a553d54df876f9f5 |
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| Source note | uspto-grants-1994_05 |
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