HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 928818Generated: October 31, 2026
Phosphorus oxychloride → HCID 86715649, compound
https://huagongshe.com/reaction/928818
Participants
| Role | Name | HCID | Charge |
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| Reactant | Phosphorus oxychloride | HCID 24813 | — |
| Reactant | HCID 178437400 | HCID 178437400 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | HCID 86715649 | HCID 86715649 | — |
Reaction Steps
A round-bottomed flask containing a mixture of 6-bromo-2-ethyl-3-(4-(trifluoromethyl)benzyl)quinolin-4-ol (4.00 g, 8.29 mmol, Intermediate 58: step b), phosphorous oxychloride (3.50 mL, 37.3 mmol) and acetonitrile (27 mL) was placed into a metal heating block at 90° C. After 65 min, the reaction mixture was cooled to room temperature. The acetonitrile and excess phosphorous oxychloride was removed by rotary evaporation. The residue was dissolved in dichloromethane (100 mL) and the solution was cooled in an ice-water bath. Ice (50 mL) was added. Concentrated aqueous ammonia solution was added dropwise until the pH=8-9 by litmus paper test. The biphasic mixture was separated and the aqueous layer was extracted with dichloromethane (50 mL). The combined organics were dried with sodium sulfate and the dried solution was filtered. Silica gel (8 g) was added to the filtrate and the solvents were removed by rotary evaporation to provide a free-flowing powder. The powder was loaded onto a silica gel column. Elution with hexanes initially, grading to 20% ethyl acetate-hexanes provided the title compound as an off-white solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09290476B2 |
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| Source dataset | uspto-grants-2016_03 |
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| ORD ID | ord-0e3be5390cfa4c4e916ced1baef4c35a |
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| Source note | uspto-grants-2016_03 |
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