HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1275539Generated: October 29, 2026
Ammonium Persulfate → HCID 22117145, compound
https://huagongshe.com/reaction/1275539
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Ammonium Persulfate | HCID 62648 | — |
| Reactant | HCID 825051 | HCID 825051 | — |
| Reactant | HCID 12218619 | HCID 12218619 | — |
| Catalyst | Silver Nitrate | HCID 24470 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | HCID 22117145 | HCID 22117145 | 46.4% |
Reaction Steps
2-Benzoyloxy-1,4-naphthoquinone (1.39 g, 5 mmol), trimethylsilylpropionic acid (1.09 g, 7.5 mmol) and silver nitrate (523 mg, 3 mmol) were suspended in 40 ml aqueous acetonitrile (1:1) and then heated to 65° C. Ammonium persulphate (1.71 g, 7.5 mmol) in 20 ml water was added slowly and dropwise over 30 minutes to the mixture. The reaction mixture was stirred at this temperature for a further hour and then cooled, diluted with diethyl ether and the aqueous phase removed. The organic extract was washed with saturated sodium bicarbonate solution, then brine and dried over anhydrous magnesium sulphate. After concentration in vacuo, the crude material was chromatographed using petroleum ether/ethyl acetate as eluent to give 2-benzoyloxy-3-(2'-trimethylsilylethyl)-1,4-naphthoquinone (879 mg) which was recrystallised from methanol, m.pt.: 92-95° C. NMR peaks at: 184.4, 178.2, 150.3, 142.6, 134.0, 133.8, 132.1, 130.9, 126.6, 126.6; 18.8, 16.2; -2.0; 163.8, 128.0, 128.7, 130.4, 134.2 (PhCO).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06162799 |
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| Source dataset | uspto-grants-2000_12 |
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| ORD ID | ord-e68e4fa1be104e00b5ec9c0d5fb52ed6 |
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| Source note | uspto-grants-2000_12 |
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