HuagongsheHuagongshe Chemistry Print Report · For research reference only
Phenyltrimethylammonium bromide dibromide → 2-Bromo-1-(3-chloro-5-(trifluoromethyl)pyridin-2-yl)ethanone
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Phenyltrimethylammonium bromide dibromide | HCID 17977687 | — |
| Reactant | 1-(3-Chloro-5-trifluoromethyl-pyridin-2-yl)-ethanone | HCID 21712136 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 2-Bromo-1-(3-chloro-5-(trifluoromethyl)pyridin-2-yl)ethanone | HCID 86057596 | — |
Reaction Steps
To a solution of 16.6 g (0.074 mol) of 1-[3-chloro-5-(trifluoromethyl)-2-pyridinyl]ethanone in 150 ml of dry tetrahydrofuran, were added portionwise at room temperature 27.8 g (0.074 mol) of phenyltrimethylammonium tribromide. The solution was stirred for 3 hours at room temperature. The formed solid was removed by filtration and the mother liquors were concentrated under vacuum. The resulting orange oil (32.7 g) was purified by flash chromatography on silica gel (eluent: heptane/dichloromethane 3:1) to give 2-bromo-1-[3-chloro-5-(trifluoromethyl)-2-pyridinyl]ethanone: 10.4 g (46%) as a yellow oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08318777B2 |
| Source dataset | uspto-grants-2012_11 |
| ORD ID | ord-b560b56f6c3241cc88b714dbc15b3c39 |
| Source note | uspto-grants-2012_11 |