HuagongsheHuagongshe Chemistry Print Report · For research reference only
Hydrochloric Acid → 1-(Benzo[d][1,3]dioxol-4-yl)piperazine hydrochloride
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Diisopropyl Ether | HCID 7914 | — |
| Reactant | 1,4-Dioxane | HCID 31275 | — |
| Reactant | Tert-butyl 4-(benzo[d][1,3]dioxol-4-yl)piperazine-1-carboxylate | HCID 68282758 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 1-(Benzo[d][1,3]dioxol-4-yl)piperazine hydrochloride | HCID 53487964 | 100% |
Reaction Steps
In a 50 mL flask, Tert-butyl 4-(benzo[d][1,3]dioxol-4-yl)piperazine-1-carboxylate (1.145 g, 3.74 mmol) was combined with dichloromethane M (20 ml) to give a colorless solution. Hydrochloric acid solution, 4M in dioxane (9.34 ml, 37.4 mmol) was added and the reaction mixture was stirred for 4 hours at room temperature. 15 ml of Diisoproylether were added and the mixture was stirred for 5 min at 0° C. The precipitate was collected by filtration, washed with 2 ml of diisopropylether and dried to yield the title compound as a white solid (0.955 grs, 100%). MS (ISP) m/z=207.4 [(M+H)+].
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08722683B2 |
| Source dataset | uspto-grants-2014_05 |
| ORD ID | ord-51d19ed78859479492b98cb2fc347ad4 |
| Source note | uspto-grants-2014_05 |