HuagongsheHuagongshe Chemistry Print Report · For research reference only
p-Bromoacetophenone → 4-Bromo-1-(1,3-dithian-2-yl)ethylbenzene
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | p-Bromoacetophenone | HCID 7466 | — |
| Reactant | Boron trifluoride etherate | HCID 8000 | — |
| Reactant | 1,3-Propanedithiol | HCID 8013 | — |
| Solvent | Chloroform | HCID 6212 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 4-Bromo-1-(1,3-dithian-2-yl)ethylbenzene | HCID 21960112 | — |
Reaction Steps
To the compound p-bromoacetophenone (36.85 g, 185 mmol) in trichloromethane (300 ml) was added 1,3-propanedithiol (25 g, 230 mmol) and boron trifluoride etherate (3 ml). The resulting mixture was stirred at room temperature for 48 hours. The mixture was diluted with dichloromethane (500 ml), washed twice with 10% sodium hydroxide (200 ml), water, and brine, and then dried (Na2SO4). The product was concentrated to an oil. A portion was stirred with ether (100 ml) and a crystalline product was formed. The crystalline product was recovered by filtration and purified by recrystallization to yield 4-bromo-1-(1,3-dithian-2-yl)ethylbenzene.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05593995 |
| Source dataset | uspto-grants-1997_01 |
| ORD ID | ord-02c6462e03d749fd9f284e5b88addf22 |
| Source note | uspto-grants-1997_01 |