HuagongsheHuagongshe Chemistry Print Report · For research reference only
Potassium Carbonate → 1-(2,3-Dihydro-benzo[1,4]dioxin-6-yl)-piperazine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 1,4-Benzodioxan-6-ylamine | HCID 89148 | — |
| Reactant | Bis(2-chloroethyl)amine hydrochloride | HCID 522769 | — |
| Solvent | Chlorobenzene | HCID 7964 | — |
| Product | 1-(2,3-Dihydro-benzo[1,4]dioxin-6-yl)-piperazine | HCID 1071338 | 30.3% |
Reaction Steps
A solution of 1,4-benzodioxan-6-amine (2.00 g, 13.2 mmol), bis-(2-choroethyl)amine hydrochloride (3.54 g, 19.8 mmol). and potassium carbonate (1.83 g, 13.2 mmol) in of 20 mL chlorobenzene is heated to reflux for 24 hours. 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 (8% methanol/methylene chloride on silica) provides 0.88 g (30%) of the desired 1-(1,4-benzodioxan-6-yl)piperazine as a white solid (m.p. 138° C., TLC Rf 0.37 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-f81ab7524ffd4ddbb6e4f91f8c423654 |
| Source note | uspto-grants-2002_11 |