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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 927983Generated: November 1, 2026

Imidazole → tert-butyl (3R)-3-(iodomethyl)pyrrolidine-1-carboxylate

https://huagongshe.com/reaction/927983

Reaction equation

Participants

RoleNameHCIDCharge
ReactantImidazoleHCID 795—
ReactantIodineHCID 807—
ReactantTriphenylphosphineHCID 11776—
Reactanttert-Butyl (3R)-3-(hydroxymethyl)pyrrolidine-1-carboxylateHCID 1514340—
SolventDiethyl EtherHCID 3283—
Solvent1,4-DioxaneHCID 31275—
Producttert-butyl (3R)-3-(iodomethyl)pyrrolidine-1-carboxylateHCID 5937136893.1%

Reaction Steps

Iodine (1.91 g) was added in portions to a vigorously stirred, ice cooled suspension of imidazole (0.681 g) and triphenylphosphine (1.97 g) in diethyl ether (12 mL). The mixture was then stirred for 10 minutes before a solution of tert butyl (R)-3-hydroxymethylpyrrolidine-1-carboxylate (1 g) in dioxane (6 mL) was added dropwise. The resulting mixture was stirred at room temperature overnight, then diluted with diethyl ether and filtered. The solid was washed with diethyl ether and the combined filtrate was evaporated to dryness. The residue was purified by chromatography on silica, eluting with a mixture of ethyl acetate and pentane with a gradient of 0-20% to give tert-butyl (R)-3-iodomethylpyrrolidine-1-carboxylate (1.44 g) as an oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09290472B2
Source datasetuspto-grants-2016_03
ORD IDord-a1aee225980442869f46cc6d9fe4f392
Source noteuspto-grants-2016_03