HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 623962Generated: October 26, 2026
Phosphorus oxychloride → 6-Bromo-2-chloro-3-(4-chlorophenoxy)-4-(trifluoromethyl)quinoline
https://huagongshe.com/reaction/623962
Participants
| Role | Name | HCID | Charge |
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| Reactant | Phosphorus oxychloride | HCID 24813 | — |
| Reactant | Diisopropylethylamine | HCID 81531 | — |
| Reactant | 6-bromo-3-(4-chlorophenoxy)-4-(trifluoromethyl)quinolin-2(1H)-one | HCID 86715448 | — |
| Product | 6-Bromo-2-chloro-3-(4-chlorophenoxy)-4-(trifluoromethyl)quinoline | HCID 86715447 | — |
Reaction Steps
To a suspension of 6-bromo-3-(4-chlorophenoxy)-4-(trifluoromethyl)quinolin-2(1H)-one (1.08 g, 2.58 mmol, Intermediate 7, step c) in phosphoryl trichloride (7.2 mL, 77.3 mmol) was added diisopropylethylamine (1.33 mL, 7.74 mmol). The resulting mixture was heated at 120° C. for 8 hours. The solution was concentrated in vacuo at room temperature and the resulting residue was cooled to 0° C. with an ice bath. To the cold residue was added ice in small portions to quench excess phosphoryl trichloride. After cessation of bubbling, the solid suspension was diluted with dichloromethane. The organic phase was separated out, dried (MgSO4), filtered and concentrated to yield the title compound.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09303015B2 |
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| Source dataset | uspto-grants-2016_04 |
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| ORD ID | ord-e19ffcb028144e6ca7ee9e4a144836dc |
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| Source note | uspto-grants-2016_04 |
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