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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1021935Generated: October 31, 2026

Imidazole → Tert-butyl 3-iodoazetidine-1-carboxylate

https://huagongshe.com/reaction/1021935

Reaction equation

Participants

RoleNameHCIDCharge
ReactantImidazoleHCID 795—
ReactantIodineHCID 807—
ReactantTriphenylphosphineHCID 11776—
ReactantSodium BicarbonateHCID 516892—
ReactantTert-butyl 3-hydroxyazetidine-1-carboxylateHCID 2756801—
SolventTolueneHCID 1140—
ProductTert-butyl 3-iodoazetidine-1-carboxylateHCID 1100052293.8%

Reaction Conditions

Temperature100 °C

Reaction Steps

A solution of tert-butyl 3-hydroxyazetidine-1-carboxylate (3.5 g, 0.020 mol) in toluene (200 mL) was treated with imidazole (4.08 g, 0.060 mol), triphenylphosphine (0.60 g, 0.040 mol), and iodine (7.62 g, 0.030 mol). The mixture was heated at 100° C. for 1 h. It was then cooled to room temperature and poured into saturated NaHCO3 solution (30 mL). Excess triphenylphosphine was destroyed by addition of iodine until iodine coloration persisted in organic layer. The mixture was washed with 5% Na2SO3 solution, dried over Na2SO4, and evaporated in vacuo. The residue was purified by silica-gel column chromatography to afford 206a (5.31 g, 93%). MS-ESI: [M+H]+ 284.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08716274B2
Source datasetuspto-grants-2014_05
ORD IDord-4c7e7f4da52f434da7e0556888f2c34e
Source noteuspto-grants-2014_05