HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 732732Generated: October 30, 2026
Ethyl Acetate → 1-{2-[4-(2-Benzyloxy-6-methoxy-naphthalen-1-yloxy)-phenoxy]-ethyl}-piperidine
https://huagongshe.com/reaction/732732
Participants
| Role | Name | HCID | Charge |
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| Reactant | Ethyl Acetate | HCID 8857 | — |
| Reactant | Cesium carbonate | HCID 10796 | — |
| Reactant | 4-[2-(Piperidin-1-yl)ethoxy]phenol | HCID 10609021 | — |
| Reactant | 2-Benzyloxy-1-bromo-6-methoxy-naphthalene | HCID 11702908 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | 1-{2-[4-(2-Benzyloxy-6-methoxy-naphthalen-1-yloxy)-phenoxy]-ethyl}-piperidine | HCID 11677433 | 30% |
Reaction Steps
Combine toluene (200 mL), 2-benzyloxy-1-bromo-6-methoxy-naphthalene (30 g, 87.4 mmol), 4-(2-piperidin-1-yl-ethoxy)phenol (23.2 g, 105 mmol) and cesium carbonate (34.4 g, 105 mmol), heat the mixture to reflux. Remove a portion of the toluene (100 mL). Add ethyl acetate (390 mg, 4.37 mmol) and copper triflate benzene complex (2.20 g, 4.37 mmol) to the reaction mixture and stir for 5 minutes. Remove the solvent by distillation and heat the resulting residue to 174° C. for 1.5 hours. Dissolve the residue in a mixture of ethyl acetate (200 mL) and aqueous HCl (1 N, 90 mL). Separate and concentrate the organics to a residue. Column chromatograph the residue to give 12.4 g of 1-{2-[4-(2-benzyloxy-6-methoxy-naphthalen-1-yloxy)-phenoxy]-ethyl}-piperidine (30%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07585977B2 |
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| Source dataset | uspto-grants-2009_09 |
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| ORD ID | ord-2ffdb352ef6c4d8bbf3995295f14c4bf |
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| Source note | uspto-grants-2009_09 |
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