HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2271521Generated: October 31, 2026
Phosphorus oxychloride → 1-(6-Bromo-4-chloroquinolin-3-yl)-3-methylbutan-1-one
https://huagongshe.com/reaction/2271521
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Phosphorus oxychloride | HCID 24813 | — |
| Reactant | Sodium bicarbonate ethyl acetate | HCID 86584982 | — |
| Reactant | HCID 178446973 | HCID 178446973 | — |
| Product | 1-(6-Bromo-4-chloroquinolin-3-yl)-3-methylbutan-1-one | HCID 86692843 | 98% |
Reaction Steps
1-(6-Bromo-4-hydroxyquinolin-3-yl)-3-methylbutan-1-one (300 mg, 0.970 mmol) was added to phosphoryl chloride (9.7 mL) and the reaction was stirred at 85° C. for 1 h. After this time the reaction mixture was cooled to room temperature and slowly poured into a 2:1 solution of satd. aq. sodium bicarbonate/ethyl acetate that was cooled to 0° C. The organic layer was separated and was washed with satd. aq. sodium bicarbonate, dried over anhydrous sodium sulfate, filtered, and concentrated under reduced pressure to afford the desired product (309 mg, 98%) as a yellow oil: 1H NMR (500 MHz, CDCl3) δ 8.86 (s, 1H), 8.51 (d, J=2.0 Hz, 1H), 8.01 (d, J=8.9 Hz, 1H), 7.91 (dd, J=8.9, 2.0 Hz, 1H), 2.96 (d, J=6.9 Hz, 2H), 2.39-2.23 (m, 1H), 1.03 (d, J=6.7 Hz, 6H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09120749B2 |
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| Source dataset | uspto-grants-2015_09 |
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| ORD ID | ord-69bcba8cbf434d79aa3a6204058a227e |
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| Source note | uspto-grants-2015_09 |
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