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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 229536Generated: October 30, 2026

Methyl iodide → HCID 57758720, compound

https://huagongshe.com/reaction/229536

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethyl iodideHCID 6328—
ReactantAmmonium ChlorideHCID 25517—
ReactantPotassium bis(trimethylsilyl)amideHCID 3251421—
ReactantHCID 68862420HCID 68862420—
SolventTetrahydrofuranHCID 8028—
ProductHCID 57758720HCID 5775872083.1%

Reaction Steps

To a solution of ethyl(3R,4R)-4-fluoromethyl-3-methyl-2-oxo-1-[(1R)-1-phenylethyl]pyrrolidine-3-carboxylate (33.4 g, 114 mmol) and iodomethane (9.94 mL, 159 mmol) in tetrahydrofuran (670 mL), potassium bistrimethylsilyl amide (274 mL, 137 mmol, 0.5M solution in toluene) was added at −78° C., and the mixture was stirred at the same temperature for 10 minutes. The temperature was gradually increased in 30 minutes with stirring to −10° C., and saturated aqueous solution of ammonium chloride (700 mL) was added to the reaction mixture. The mixture was extracted with ethyl acetate (700 mL×2), and the organic layer was washed with saturated aqueous solution of sodium chloride (500 mL), and dried with anhydrous sodium sulfate. After filtration, the filtrate was concentrated under reduced pressure, and the residue was purified by silica gel column chromatography (elusion by hexane:ethyl acetate, 7:1→1:1) to obtain 29.1 g (83%) of the title compound as a pale yellow oily substance.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07563805B2
Source datasetuspto-grants-2009_07
ORD IDord-0f76348675f147148409824eb8bbe07c
Source noteuspto-grants-2009_07