HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 627473Generated: October 27, 2026
Sodium Hydroxide → 4-Chloro-6-iodo-3-phenyl-2-(trifluoromethyl)quinoline
https://huagongshe.com/reaction/627473
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | Ammonium Hydroxide | HCID 14923 | — |
| Reactant | Phosphorus oxychloride | HCID 24813 | — |
| Reactant | HCID 178515324 | HCID 178515324 | — |
| Product | 4-Chloro-6-iodo-3-phenyl-2-(trifluoromethyl)quinoline | HCID 86716064 | — |
Reaction Steps
A solution of 6-iodo-3-phenyl-2-(trifluoromethyl)quinolin-4-ol (1.54 g, 3.71 mmol, Intermediate 5, step a) in phosphoryl trichloride (5 mL, 53.8 mmol) was heated at 110° C. for 1 hour 45 min, and then cooled to room temperature. Ice-water was added, and the mixture was basified at 4° C. with 50% NaOH and conc. NH4OH until pH 9. The precipitated solid was filtered, washed with water and Et2O, and dried to provide the title compound. The filtrate was separated and the aqueous layer was extracted with CH2Cl2. The combined organic phases were dried (Na2SO4), filtered, concentrated, and purified by flash column chromatography (80 g silica gel column, 0-5% EtOAc in heptane), affording a mixture of the title compound and des-iodo by-product in about 8:1 ratio as a thick oil, which solidified overnight.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09309222B2 |
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| Source dataset | uspto-grants-2016_04 |
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| ORD ID | ord-982698da522f4d6ba63d9ffbdc63b5b6 |
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| Source note | uspto-grants-2016_04 |
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