HuagongsheHuagongshe Chemistry Print Report · For research reference only
Propargyl bromide → 1-Methyl-4-(prop-2-yn-1-yl)piperazine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Propargyl bromide | HCID 7842 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 1-Methylpiperazine | HCID 53167 | — |
| Solvent | Acetone | HCID 180 | — |
| Product | 1-Methyl-4-(prop-2-yn-1-yl)piperazine | HCID 13514091 | 51% |
Reaction Steps
A solution of 3-bromoprop-1-yne (1.70 mL, 22.5 mmol in acetone (7 mL) was added to a suspension of 1-methylpiperazine (3.77 mL, 33.7 mmol) and K2CO3 (4.66 g, 33.7 mmol) in acetone (40 mL) at 0° C. The mixture was stirred at room temperature for 4 h and then filtered. The filtrate was evaporated to dryness and the residue was taken up with water (80 mL) and extracted with DCM (2×20 mL). The separated organic phase was washed with brine (3×5 mL), dried over sodium sulfate and evaporated to afford the title compound as brown oil (1.60 g, 51%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08912200B2 |
| Source dataset | uspto-grants-2014_12 |
| ORD ID | ord-f5fd91c89f6e46609417f5d6eb4a5723 |
| Source note | uspto-grants-2014_12 |