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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1042093Generated: November 1, 2026

Tetrahydrofuran → HCID 66726067, compound

https://huagongshe.com/reaction/1042093

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTetrahydrofuranHCID 8028—
ReactantPotassium hydroxy sulfiteHCID 23707502—
ReactantHCID 66726142HCID 66726142—
SolventMethanolHCID 887—
SolventWaterHCID 962—
ProductHCID 66726067HCID 6672606798%

Reaction Steps

2-(Benzyloxy)-4-[4-(methylthio)phenoxy]-1-nitrobenzene (10.3 g) was dissolved in a mixed solvent of tetrahydrofuran (200 mL)-methanol (100 mL)-water (50 mL), Oxone (trade mark) (42.0 g) was added under ice-cooling, and the mixture was stirred at room temperature for 4 hr. The reaction solution was filtered to remove a white solid, and the filtrate was concentrated. Water was added to the residue, and the mixture was extracted with ethyl acetate. The organic layer was washed successively with water and saturated brine, dried over magnesium sulfate, filtered and concentrated under reduced pressure. The obtained solid was washed with a diethyl ether-hexane mixed solvent to give the title compound (11.0 g, yield 98%) as pale-yellow crystals.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08557805B2
Source datasetuspto-grants-2013_10
ORD IDord-e07e0ab906d84d4ca35cd980a8eebb53
Source noteuspto-grants-2013_10