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
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Imidazole | HCID 795 | — |
| Reactant | Iodine | HCID 807 | — |
| Reactant | Triphenylphosphine | HCID 11776 | — |
| Reactant | (S)-1-Benzyl-5-hydroxymethyl-2-pyrrolidinone | HCID 10442943 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | (S)-5-iodomethyl-1-(phenylmethyl)-2-pyrrolidinone | HCID 10425818 | — |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05981546 |
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| Source dataset | uspto-grants-1999_11 |
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| ORD ID | ord-ade771d594714a41b90c20ba94b611b2 |
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| Source note | uspto-grants-1999_11 |
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