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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 441053Generated: October 26, 2026

Methyl iodide → 5,7-Bis(methoxymethoxy)-2-methylthiochromone

https://huagongshe.com/reaction/441053

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethyl iodideHCID 6328—
ReactantCarbon DisulfideHCID 6348—
Reactant18-Crown-6HCID 28557—
ReactantPotassium hydrideHCID 82127—
Reactant1-[2-Hydroxy-4,6-bis(methoxymethoxy)phenyl]ethanoneHCID 10879697—
SolventWaterHCID 962—
SolventTetrahydrofuranHCID 8028—
Product5,7-Bis(methoxymethoxy)-2-methylthiochromoneHCID 5708550791.6%

Reaction Steps

Under cooling on ice, potassium hydride (0.5 ml of 35% mineral oil) was suspended in 2 ml THF. 2 ml of 126 mg of 2'-hydroxy-4',6'-bis(methoxymethoxy)acetophenone (0.492 mmol) and 130 mg of 18-crown-6 (0.492 mmol) in THF was added dropwise to the above suspension, and the mixture was stirred for 1 hour. After addition of 0.89 ml of carbon disulfide (14.76 mmol), the solution was stirred for 20 hours at room temperature. Then, 0.5 ml of methyl iodide was added thereto, and the solution was stirred for 30 min. After water was slowly added thereto, the reaction solution was extracted twice with ether, and the organic layer was washed with saturated NaCl water and then dried over sodium sulfate anhydride. The solvent was distilled off and the resulting crude product was washed with hexane, to give 133.5 mg of 5,7-bis(methoxymethoxy)-2-methylthiochromone (87% yield).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05521216
Source datasetuspto-grants-1996_05
ORD IDord-81be17509c404bde932adfb2225d6ac0
Source noteuspto-grants-1996_05