HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1923481Generated: October 30, 2026
Potassium Carbonate → HCID 18413140, compound
https://huagongshe.com/reaction/1923481
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 1-Methylpiperazine | HCID 53167 | — |
| Reactant | 1-Bromo-4-chlorobutane | HCID 81364 | — |
| Solvent | Acetone | HCID 180 | — |
| Product | HCID 18413140 | HCID 18413140 | 48.5% |
Reaction Steps
In a 2 L three-necked round bottomed flask was added N-methyl-piperazine (100.16 g, 1.0 mol), acetone (1000 mL), and anhydrous potassium carbonate (276.42 g, 2.0 mol, 2.0 equiv.). The flask was equipped with a mechanical stirrer and a condenser. 4-chloro-1-bromo-butane (188.6 g, 1.1 mol, 1.1 equiv.) was added dropwise under continuous stirring at room temperature over a period of 30 min. The suspension mixture was then stirred at 40° C. The progress of the reaction was monitored by TLC, which confirmed the reaction was completed after 4 hours. The mixture was cooled to room temperature and the insoluble materials were removed by filtration and washed with dichloromethane (2×100 mL). The combined filtrates were concentrated under vacuum until they became dry. The residue was then mixed with dichloromethane (500 mL). Insoluble materials were removed by filtration and washed by dichloromethane (2×100 mL). The combined filtrate and washings were concentrated and purified through a flash silica gel column, which gave the expected product as light yellow oil. (92.5 g, 48.5% yield).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08178527B2 |
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| Source dataset | uspto-grants-2012_05 |
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| ORD ID | ord-7ad73db038d34a97bcbcdd2e3ff4e912 |
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| Source note | uspto-grants-2012_05 |
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