HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1385200Generated: October 31, 2026
Sulfuric Acid → 2-(4-Fluorophenyl)naphtho[2,3-d]oxazole-4,9-dione
https://huagongshe.com/reaction/1385200
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Sulfuric Acid | HCID 1118 | — |
| Reactant | Diethyl Ether | HCID 3283 | — |
| Reactant | 2-Amino-3-chloro-1,4-naphthoquinone | HCID 17748 | — |
| Reactant | 4-Fluorobenzoyl chloride | HCID 67879 | — |
| Solvent | Nitrobenzene | HCID 7416 | — |
| Product | 2-(4-Fluorophenyl)naphtho[2,3-d]oxazole-4,9-dione | HCID 2307331 | 33% |
Reaction Steps
To a solution of 6.22 g (30 mmol) of 2-amino-3-chloro-1,4-dihydro-1,4-dioxo-naphthalene in 60 mL of nitrobenzene, 18.00 mL (150 mmol) of 4-fluorobenzoic acid chloride are added with protection from light. After 10 min of stirring with reflux, 0.20 mL of concentrated sulfuric acid is added. After 12 h and complete cooling, ether is added to obtain a yellow precipitate which is filtered through fritted glass, washed with ether and purified on a flash column (support: silica; conditioning: heptane; eluant: dichloromethane/heptane, 60/40). The yellow powder obtained after evaporation of the solvent is uncolored, recrystallized in dichloromethane to produce 2.90 g of 4,9-dihydro-4,9-dioxo-2-(4-fluorophenyl)-naphtho[2,3-d]oxazole in the form of yellow crystals.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06262095B1 |
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| Source dataset | uspto-grants-2001_07 |
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| ORD ID | ord-02ec5a519ad14f02be13d55a4908bc37 |
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| Source note | uspto-grants-2001_07 |
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