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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1602648Generated: October 26, 2026

Imidazole → (S)-5-iodomethyl-1-(phenylmethyl)-2-pyrrolidinone

https://huagongshe.com/reaction/1602648

Reaction equation

Participants

RoleNameHCIDCharge
ReactantImidazoleHCID 795—
ReactantIodineHCID 807—
ReactantTriphenylphosphineHCID 11776—
Reactant(S)-1-Benzyl-5-hydroxymethyl-2-pyrrolidinoneHCID 10442943—
SolventDiethyl EtherHCID 3283—
SolventAcetonitrileHCID 6342—
Product(S)-5-iodomethyl-1-(phenylmethyl)-2-pyrrolidinoneHCID 10425818—

Reaction Conditions

Temperature50 °C

Reaction Steps

To a solution of 13-1 (18.5 g, 90.1 mmol), triphenylphosphine (40.1 g, 153 mmol), and imidazole (11.03 g, 162 mmol) in 225 mnL of acetonitrile and 150 mL of ether at 0° C. was added iodine (34.3 g, 135 mmol) in 5 portions over 5 minutes. After 10 minutes, the reaction was heated to 50° C., and a stream of argon passed over the reaction to purge the evaporating ether. After an additional 30 minutes, the mixture was diluted with ether, the organic layer washed with NaHCO3 (sat.) and brine, dried over K2CO3, and the solvent evaporated. Flash chromatography of the residue (silica, 7-15% EtOAc/CHCl3) gave 13-2 as a yellow oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05981546
Source datasetuspto-grants-1999_11
ORD IDord-ade771d594714a41b90c20ba94b611b2
Source noteuspto-grants-1999_11