HuagongsheHuagongshe Chemistry Print Report · For research reference only
Piperonyl alcohol → 1,3-Benzodioxole, 5-(bromomethyl)-
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Piperonyl alcohol | HCID 10322 | — |
| Reactant | Phosphorus tribromide | HCID 24614 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Product | 1,3-Benzodioxole, 5-(bromomethyl)- | HCID 6451423 | 182% |
Reaction Steps
To a solution of piperonyl alcohol (5.0 g, 32.86 mmol) in anhydrous diethyl ether (80 mL) was added PBr3 (1.56 mL, 16.43 mmol) in one portion, and the resulting mixture was stirred at room temperature for 3 hours. The mixture was diluted with diethyl ether (100 mL) and washed with H2O (2×50 mL), saturated NaHCO3 (2×50 mL), and brine (2×50 mL). The ether layer was dried over anhydrous MgSO4, and the solvent was removed under reduced pressure to afford piperonyl bromide (6.43 g, 91%) as a yellow-grey solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06458829B1 |
| Source dataset | uspto-grants-2002_10 |
| ORD ID | ord-74c4b8e1b676453ab76b3e6ac6b94f5b |
| Source note | uspto-grants-2002_10 |