HuagongsheHuagongshe Chemistry Print Report · For research reference only
Boron trifluoride → HCID 86710507, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Boron trifluoride | HCID 6356 | — |
| Reactant | Sodium Carbonate | HCID 10340 | — |
| Reactant | 1,2-Ethanedithiol | HCID 10902 | — |
| Reactant | HCID 86710508 | HCID 86710508 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 86710507 | HCID 86710507 | — |
Reaction Steps
At 0° C., ethane-1,2-dithiol (3 mL) and BF3.2HOAc (4.8 mL) were added into a solution of (5-bromo-2-chlorophenyl)(4-(2,2,2-trifluoroethoxy)phenyl)methanone (5.0 g) in dry DCM. The mixture was stirred at room temperature for 12 hours. The mixture was added with saturated Na2CO3 aqueous solution and then extracted with DCM. The organic phases were combined, dried over Na2SO4, and concentrated to obtain the crude product, then the crude product was purified by silica-gel column chromatography (PE/EA=200/1) to obtain 4 g of 2-(5-bromo-2-chlorophenyl)-2-(4-(2,2,2-trifluoroethoxy)phenyl)-1,3-dithiolane.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08957033B2 |
| Source dataset | uspto-grants-2015_02 |
| ORD ID | ord-55ebf8b81deb4cca84bcb04b8117e8d9 |
| Source note | uspto-grants-2015_02 |