HuagongsheHuagongshe Chemistry Print Report · For research reference only
Boron trifluoride etherate → 2-tert-Butyl-4-(pyrid-3-yl)-5-(2-bromophenyl)-1,3-dioxolane
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Boron trifluoride etherate | HCID 8000 | — |
| Reactant | Pivalaldehyde | HCID 12417 | — |
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Reactant | 1-(Pyrid-3-yl)-2-(2-bromophenyl)-ethanediol | HCID 19774197 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 2-tert-Butyl-4-(pyrid-3-yl)-5-(2-bromophenyl)-1,3-dioxolane | HCID 19774199 | — |
Reaction Steps
8 g (0.027 mol) of 1-(pyrid-3-yl)-2-(2-bromophenyl)-ethanediol and 4.5 g (0.0525 mol) of pivaldehyde were dissolved in 100 ml of methylene chloride. This was achieved by adding 4.35 ml (0.0525 mol) of boron trifluoride etherate dropwise at room temperature and stirring overnight. Thereafter, the mixture was poured onto ice water and was neutralized with NaHCO3 solution. The organic phase was washed with water, dried over Na2SO4 and filtered, and the filtrate was evaporated down. The crude product was purified by chromatography.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05194441 |
| Source dataset | uspto-grants-1993_03 |
| ORD ID | ord-fd7d379506b446dc8fd996a227ed1ff7 |
| Source note | uspto-grants-1993_03 |