HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 655598Generated: October 26, 2026
Sodium Iodide → 4-[2-(3,4-Dimethoxy-phenyl)-ethyl]-piperazine-1-carboxylic acid t-butyl ester
https://huagongshe.com/reaction/655598
Participants
| Role | Name | HCID | Charge |
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| Reactant | Sodium Iodide | HCID 5238 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | tert-Butyl piperazine-1-carboxylate | HCID 143452 | — |
| Reactant | 4-(2-Chloroethyl)-1,2-dimethoxybenzene | HCID 3015359 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | 4-[2-(3,4-Dimethoxy-phenyl)-ethyl]-piperazine-1-carboxylic acid t-butyl ester | HCID 66995785 | 76.5% |
Reaction Steps
A reaction mixture of 4-(2-chloroethyl)-1,2-dimethoxybenzene (3.6 g, 17.9 mmol), piperazine-1-carboxylic acid t-butyl ester (4.0 g, 21.5 mmol), K2CO3 (4.97 g, 36 mmol), and NaI (2.7 g, 18 mmol) in DMF (20 mL) was stirred at 80° C. for 3 h, cooled to room temperature, and partitioned between water and ethyl acetate. The organic layer was washed with water and brine, dried over anhydrous sodium sulfate, and concentrated. The residue was purified by column chromatography to afford 4-[2-(3,4-dimethoxy-phenyl)-ethyl]-piperazine-1-carboxylic acid t-butyl ester (4.8 g, 76%) which was dissolved in 4 N HCl in dioxane. This solution was stirred at room temperature for 4 h, concentrated, and dried in a high vacuum oven to give the title compound quantitatively.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08071602B2 |
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| Source dataset | uspto-grants-2011_12 |
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| ORD ID | ord-5f9829d032d24b5a9f7bd5cfe5515bc6 |
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| Source note | uspto-grants-2011_12 |
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