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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1271140Generated: November 3, 2026

Tetrahydrofuran → 1-(1-Ethylpropyl)-5-methyl-3-(methylsulfonyl)-2(1H)-pyrazinone

https://huagongshe.com/reaction/1271140

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTetrahydrofuranHCID 8028—
ReactantPotassium hydroxy sulfiteHCID 23707502—
Reactant1-(1-Ethylpropyl)-5-methyl-3-(methylthio)-2 (1H)-pyrazinoneHCID 58845171—
SolventWaterHCID 962—
SolventEthyl AcetateHCID 8857—
Product1-(1-Ethylpropyl)-5-methyl-3-(methylsulfonyl)-2(1H)-pyrazinoneHCID 5884517367%

Reaction Conditions

Temperature25 °C

Reaction Steps

A solution of XXXII (200 mg, 0.9 mmol) in THF (25 mL) was treated with Oxone™ (1.1 g, 1.8 mmol) portionwise as a solid at 25° C. The reaction mixture was stirred at 25° C. for 16 h and diluted with water (20 mL) and ethyl acetate (25 mL). The organic phase was dried (MgSO4), filtered, and concentrated in vacuo to give the product XXXIII (153 mg, 67%) as a yellow oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07205306B2
Source datasetuspto-grants-2007_04
ORD IDord-4e23d85e738f427bb2cd3f2727181f6d
Source noteuspto-grants-2007_04