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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 495201Generated: October 29, 2026

Iodine → HCID 86610529, compound

https://huagongshe.com/reaction/495201

Reaction equation

Participants

RoleNameHCIDCharge
ReactantIodineHCID 807—
ReactantSodium ThiosulfateHCID 24477—
ReactantBis(trifluoroacetoxy)iodobenzeneHCID 102317—
ReactantHCID 68419954HCID 68419954—
SolventWaterHCID 962—
SolventDichloromethaneHCID 6344—
ProductHCID 86610529HCID 8661052996%

Reaction Conditions

Temperature-30 °C

Reaction Steps

Methyl 3,5-bis (methoxymethoxy)-2-(4-methoxybenzoyl)phenylacetate (0.75 g, 1.9 mmol) obtained in Example 134, Step 2 was dissolved in dichloromethane (20 mL). The resulting solution was cooled to −30° C., and iodine (0.47 g, 1.9 mmol) and [bis(trifluoroacetoxy)iodo]benzene (0.8 g, 1.9 mmol) were successively added thereto in an atmosphere of argon, followed by stirring for 2 hours. To the reaction mixture was added a saturated aqueous solution of sodium thiosulfate, and the mixture was further stirred for one hour, while the temperature was raised to room temperature. To the reaction mixture was added water for liquid separation, and the aqueous layer was extracted with ethyl acetate. The organic layers were combined, dried over anhydrous sodium sulfate, and then concentrated under reduced pressure. The resulting, residue was purified by silica gel column chromatography (ethyl acetate/hexane=1/4-1/2) to obtain methyl 3,5-bis(methoxymethoxy)-2-iodo-6-(4-methoxybenzoyl)phenylacetate (0.95 g, 96%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07538224B2
Source datasetuspto-grants-2009_05
ORD IDord-5a9a22eb025f420f9bcd8d15d0edbf96
Source noteuspto-grants-2009_05