HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 422725Generated: October 31, 2026
Phosphorus oxychloride → 4,7-Dichloro-2-phenylquinazoline
https://huagongshe.com/reaction/422725
Participants
| Role | Name | HCID | Charge |
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| Reactant | Phosphorus oxychloride | HCID 24813 | — |
| Reactant | 7-Chloro-2-phenylquinazolin-4(3H)-one | HCID 135431223 | — |
| Product | 4,7-Dichloro-2-phenylquinazoline | HCID 362506 | — |
Reaction Steps
7-Chloro-2-phenylquinazolin-4(3H)-one (3.11 g, 12.1 mmol) in POCl3 (40 mL) was heated with stirring at 90° C. under N2 for 2 d. The reaction was cooled to rt and evaporated to dryness under high vacuum. The residue was stirred for 30 min at 0° C. under Ar as a suspension in NH3/i-PrOH (2 M, 45 mL). Later DCM (˜100 mL) was added and stirring was continued for 1 h at rt. Aq NH4OH (conc, 50 mL) was added and layers were separated. The aqueous layer was extracted with DCM (2×). The organic phase was washed (satd NaHCO3, H2O, brine), dried (Na2SO4) and concentrated under reduced pressure to provide the title compound as a light yellow solid; 1H NMR (400 MHz, CD2Cl2) δ 8.56-8.46 (m, 2H), 8.14 (d, J=9.2 Hz, 1H), 8.02 (d, J=2.4 Hz, 1H), 7.56 (dd, J=2.4 Hz, 9.2 Hz, 1H), 7.52-7.45 (m, 3H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08101613B2 |
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| Source dataset | uspto-grants-2012_01 |
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| ORD ID | ord-ad60310677344dfbb3c65dc4c1b67b91 |
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| Source note | uspto-grants-2012_01 |
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