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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1824959Generated: October 31, 2026

Methyl iodide → HCID 22144818, compound

https://huagongshe.com/reaction/1824959

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethyl iodideHCID 6328—
ReactantLithium diisopropylamideHCID 2724682—
ReactantEthyl 2-(5-fluorobenzofur-7-yl)acetateHCID 22144764—
SolventTetrahydrofuranHCID 8028—
SolventEthyl AcetateHCID 8857—
ProductHCID 22144818HCID 2214481862.5%

Reaction Conditions

Temperature-78 °C

Reaction Steps

A solution of 1.09 gm (4.90 mMol) ethyl 2-(5-fluorobenzofur-7-yl)acetate in 5 mL tetrahydrofuran was cooled to −78° C. To this solution were slowly added 6.1 mL (6.13 mMol) lithium diisopropylamide (1.0 M in tetrahydrofuran) and the mixture was stirred at −78° C. for 1 hour. To this solution were then added 0.76 mL (12.25 mMol) iodomethane and the mixture was allowed to warm to room temperature over 1 hour. The reaction mixture was then diluted with ethyl acetate and the resulting solution washed sequentially with water, saturated aqueous sodium bicarbonate, and saturated aqueous sodium chloride. The remaining organic phase was concentrated under reduced pressure and the residue subjected to flash silica gel chromatography, eluting with hexane containing 20% ethyl acetate. Fractions containing product were combined and concentrated under reduced pressure to provide 0.723 gm (62%) of the desired compound.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07045545B1
Source datasetuspto-grants-2006_05
ORD IDord-383c0921a59a45feabed8c372fb05b3d
Source noteuspto-grants-2006_05