HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 50655Generated: October 25, 2026
1-(2-Methoxyphenyl)piperazine → 3-[4-(2-Methoxy-phenyl)-piperazin-1-ylmethyl]-piperidine-1-carboxylic acid tert-butyl ester
https://huagongshe.com/reaction/50655
Participants
| Role | Name | HCID | Charge |
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| Reactant | 1-(2-Methoxyphenyl)piperazine | HCID 1346 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | tert-Butyl 3-(((methylsulfonyl)oxy)methyl)piperidine-1-carboxylate | HCID 22647269 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | 3-[4-(2-Methoxy-phenyl)-piperazin-1-ylmethyl]-piperidine-1-carboxylic acid tert-butyl ester | HCID 21303201 | — |
Reaction Steps
To a solution of 3-methanesulfonyloxymethyl-piperidine-1-carboxylic acid tert-butyl ester (11.06 g, 0.04 mol) in acetonitrile (180 mL) was added potassium carbonate (26 g, 0.19 mol) followed by 1-(2-methoxy-phenyl) piperazine (7.25 g, 0.04 mol). After completion of addition the reaction mixture was heated to reflux. After 12 h the reaction mixture was cooled down to room temperature and quenched with water. The aqueous layer was extracted with ethyl acetate (3×100 mL). The combined organic layers were dried over sodium sulfate and concentrated to yield an oil. This crude material was purified using silica gel chromatography (7:3:0.05 Hexane:EtOAc:2M NH3 in EtOH) to afford the desired compound in good yield (8.0 g, 55%). C22H35N3O3,LRMS (m/z)=390 (MH+).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06713479B2 |
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| Source dataset | uspto-grants-2004_03 |
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| ORD ID | ord-8ae9b22ad09f41dfbaab188226486b1d |
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| Source note | uspto-grants-2004_03 |
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