HuagongsheHuagongshe Chemistry Print Report · For research reference only
Potassium Carbonate → 1-(3,4-Dihydro-2H-1-benzopyran-6-yl)piperazine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | Bis(2-chloroethyl)amine hydrochloride | HCID 522769 | — |
| Reactant | 3,4-Dihydro-2H-1-benzopyran-6-amine | HCID 13297891 | — |
| Solvent | Chlorobenzene | HCID 7964 | — |
| Product | 1-(3,4-Dihydro-2H-1-benzopyran-6-yl)piperazine | HCID 15485010 | — |
Reaction Steps
A solution of 6-aminochroman from part 2 of this example (0.300 g, 2.013 mmol), bis-(2-choroethyl)amine hydrochloride (0.539 g, 3.020 mmol) and potassium carbonate (0.278 g, 2.013 mmol) in 10 mL chlorobenzene is heated at reflux for 24 h. The dark brown reaction mixture is then partitioned between 3N NaOH and methylene chloride. The organic layer is separated, dried over Mg2SO4, filtered and concentrated. Purification by flash column chromatography (5% methanol-methylene chloride) affords 0.157 g (36%) of 1-(chroman-6-yl)piperazine as a white solid, TLC Rf 0.35 (elution with 10% methanol-methylene chloride).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06486164B2 |
| Source dataset | uspto-grants-2002_11 |
| ORD ID | ord-72781df9a31a4fabbd84c58c434cfe1a |
| Source note | uspto-grants-2002_11 |