HuagongsheHuagongshe Chemistry Print Report · For research reference only
Phosphorus oxychloride → 6-Bromo-4-chloro-3-(methylsulfonyl)quinoline
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Phosphorus oxychloride | HCID 24813 | — |
| Reactant | Sodium bicarbonate ethyl acetate | HCID 86584982 | — |
| Reactant | HCID 178504827 | HCID 178504827 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 6-Bromo-4-chloro-3-(methylsulfonyl)quinoline | HCID 66715245 | 59% |
Reaction Conditions
| Temperature | 100 °C |
|---|
Reaction Steps
6-Bromo-3-(methylsulfonyl)quinolin-4-ol (573 mg, 1.90 mmol) was added to phosphoryl chloride (19 mL) and the reaction was stirred at 100° C. 16 h. Additional THF (5 mL) was added and the reaction mixture was stirred at 100° C. for 4 h. The reaction mixture was cooled and slowly poured into a 2:1 solution of satd. aq sodium bicarbonate/ethyl acetate that was pre-cooled to 0° C. The layers were separated and the aqueous layer was extracted with ethyl acetate. The combined organic layers were washed with satd. aq.sodium bicarbonate, dried over anhydrous sodium sulfate, filtered, and concentrated to afford the desired product (360 mg, 59%) as a white solid: ESI MS m/z 321 [C10H7BrClNO2S+H]+.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US09120749B2 |
| Source dataset | uspto-grants-2015_09 |
| ORD ID | ord-e820920cb8ea4ce69daa5adcf6cebc3c |
| Source note | uspto-grants-2015_09 |