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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 975692Generated: October 28, 2026

Methyl iodide → HCID 57036803, compound

https://huagongshe.com/reaction/975692

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethyl iodideHCID 6328—
ReactantEthyl AcetateHCID 8857—
ReactantPotassium CarbonateHCID 11430—
ReactantHCID 86750461HCID 86750461—
SolventWaterHCID 962—
SolventAcetonitrileHCID 6342—
ProductHCID 57036803HCID 5703680363.7%

Reaction Steps

To a solution of (2R,4S)-1-allyloxycarbonyl-2-thiocarbamoylmethyl-4-(triphenylmethylthio) pyrrolidine (110 mg) in acetonitrile (4 ml) were added iodomethane (497 mg) and potassium carbonate (61 mg). After stirring at room temperature for 3 hours, the solution was poured into a mixture of ethyl acetate and water. The separated organic layer was washed with aqueous sodium chloride solution, dried over magnesium sulfate and evaporated. The residue was subjected to column chromatography on silica gel (eluent; n-hexane:ethyl acetate=3:2) to give (2R,4S)-1-allyloxycarbonyl-2-(2-imino-2-methylthioethyl)-4(triphenylmethylthio) pyrrolidine (72 mg).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05608056
Source datasetuspto-grants-1997_03
ORD IDord-5c8b3c59d68f47c08f9bc62244c013fb
Source noteuspto-grants-1997_03