HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 268704Generated: October 26, 2026
Piperidine → Ethyl 4-(3-Piperidin-1-ylpropoxy)benzoate
https://huagongshe.com/reaction/268704
Participants
| Role | Name | HCID | Charge |
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| Reactant | Piperidine | HCID 8082 | — |
| Reactant | Sodium Carbonate | HCID 10340 | — |
| Reactant | Ethyl 4-(3-chloropropoxy)benzoate | HCID 18348522 | — |
| Catalyst | Potassium Iodide | HCID 4875 | — |
| Solvent | 1-Butanol | HCID 263 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | Ethyl 4-(3-Piperidin-1-ylpropoxy)benzoate | HCID 17986307 | — |
Reaction Steps
A stirred mixture of ethyl 4-(3-chloropropoxy)benzoate (70.0 g), piperidine (43.35 ml), sodium carbonate (45.36 g) and potassium iodide (2.37 g) in 1-butanol (650 ml) was heated at 105° C. for 16 h. The reaction was cooled to rt, diluted with EtOAc (1600 ml), washed with water (3×700 ml), saturated brine (700 ml), dried (MgSO4) and evaporated to give the title compound (D1) (82.57 g) which displayed MS and 1H NMR spectra that were identical to those of the product obtained by D1 (Method A).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07446103B2 |
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| Source dataset | uspto-grants-2008_11 |
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| ORD ID | ord-94fe1cbe5b864289ae81f3f0848c2cf1 |
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| Source note | uspto-grants-2008_11 |
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