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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2294682Generated: October 30, 2026

Potassium Persulfate → HCID 86751630, compound

https://huagongshe.com/reaction/2294682

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium PersulfateHCID 24412—
ReactantSodium ethoxideHCID 2723922—
ReactantEthyl 2-benzylacrylateHCID 11084648—
ReactantTert-butyl N-(2-methyl-2-sulfanylpropyl)carbamateHCID 45092056—
SolventWaterHCID 962—
Solvent1,4-DioxaneHCID 31275—
ProductHCID 86751630HCID 8675163072.6%

Reaction Steps

10.2 ml (11 mmol) of 1.08N sodium ethylate solution are added dropwise at 0° to a mixture of 1.99 g (10.47 mmol) of ethyl α-benzylacrylate and 2.26 g (11 mmol) of tert-butyl [2-methyl-2-mercaptopropyl]carbamate in 5 ml of dioxan. Thereafter, the mixture is stirred at 0° for 0.5 hours and at room temperature for 2.5 hours. The reaction mixture is treated while cooling with ice with 8.96 g (14.6 mmol) of potassium monopersulphate triple salt, suspended in 15 ml of water, and stirred at room temperature for 1 hour. Thereafter, the mixture is cooled to 0° and a suspension of 8.96 g (14.6 mmol) of potassium monopersulphate triple salt in 15 ml of water is again added. Subsequently, the mixture is stirred at room temperature for 15 hours. The reaction mixture is diluted with 50 ml of water and the aqueous solution is extracted three times with 50 ml of ether each time. The combined organic solutions are dried over sodium sulphate and evaporated. There are obtained 3.25 g of tert-butyl [2-[[(RS)-2-(ethoxycarbonyl)-3-phenylpropyl]sulphonyl]-2-methylpropyl]carbamate as a colourless oil; MS: 445 (M+NH4)+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05688946
Source datasetuspto-grants-1997_11
ORD IDord-d1162822fc2c4c669138a4d4fe1c6555
Source noteuspto-grants-1997_11