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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 592866Generated: October 30, 2026

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

https://huagongshe.com/reaction/592866

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 numberUS09238655B2
Source datasetuspto-grants-2016_01
ORD IDord-f8d6b780a2b443e7898ba34e7df34614
Source noteuspto-grants-2016_01