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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1275539Generated: October 29, 2026

Ammonium Persulfate → HCID 22117145, compound

https://huagongshe.com/reaction/1275539

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAmmonium PersulfateHCID 62648—
ReactantHCID 825051HCID 825051—
ReactantHCID 12218619HCID 12218619—
CatalystSilver NitrateHCID 24470—
SolventWaterHCID 962—
SolventDiethyl EtherHCID 3283—
SolventAcetonitrileHCID 6342—
ProductHCID 22117145HCID 2211714546.4%

Reaction Conditions

Temperature65 °C

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06162799
Source datasetuspto-grants-2000_12
ORD IDord-e68e4fa1be104e00b5ec9c0d5fb52ed6
Source noteuspto-grants-2000_12