HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 567681Generated: October 26, 2026
Hydrochloric Acid → 2-(2,6-Difluoro-phenyl)-8-hydroxy-benzo[d][1,3]oxazin-4-one
https://huagongshe.com/reaction/567681
Participants
| Role | Name | HCID | Charge |
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| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | 2,6-Difluorobenzoyl chloride | HCID 87438 | — |
| Reactant | 6-Acetamido-(2,6-difluoro-phenyl)-benzo[d][1,3]oxazin-4-one | HCID 9948813 | — |
| Reactant | HCID 21262505 | HCID 21262505 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Solvent | Toluene triethylamine | HCID 22504574 | — |
| Product | 2-(2,6-Difluoro-phenyl)-8-hydroxy-benzo[d][1,3]oxazin-4-one | HCID 9838451 | — |
Reaction Steps
3-Triisopropylsilyloxyanthranilic acid (0.8 g), 2,6-difluorobenzoyl chloride (0.71 mL) and triethyl amine/toluene (1/1) (25 mL) were reacted as described under (10). Reaction time 2 days. Extraction between ethyl acetate (100 mL) and HCl (1N,100 mL), followed by separation of the organic layer, drylng over MgSO4, filtering and evaporation gave a crude product which was dissolved in warm THF (20 mL) and precipitated with hexane. The resulting mixture was further purified on a silicagel column using dichloromethane as eluent. The isolated fraction (80 mg) was hydrolysed with 1% HCl in ethanol by stirring for 2 days at RT, and further hydrolysis after addition of HCl (4N, 5 mL) and ethyl acetate (10 mL). The organic layer was separated, evaporated and dried resulting in 2-(2,6-difluoro-phenyl)-8-hydroxy-benzo[d][1,3]oxazin-4-one (32 mg), mp.190-198. LC-MS showed the purity 86% with the corresponding O-triisopropylsilylated product as the impurity.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06180625B2 |
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| Source dataset | uspto-grants-2001_01 |
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| ORD ID | ord-a184ea4c4a6b4c92bf8258b1217fc931 |
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| Source note | uspto-grants-2001_01 |
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