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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2262613Generated: October 29, 2026

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

https://huagongshe.com/reaction/2262613

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 1100052295%

Reaction Conditions

Temperature100 °C

Reaction Steps

A solution of 3-hydroxy-azetidine-1-carboxylic acid tert-butyl ester (3.35 g, 19.34 mmol) in toluene (200 ml) was treated with imidazole (3.95 g, 58.01 mmol), triphenylphosphine (10.14 g, 38.65 mmol) and I2 (7.36 g, 28.99 mmol). The mixture was heated at 100° C. for 1 h, cooled down to room temperature and next poured into saturated aqueous NaHCO3 (30 ml). Excess triphenylphosphine was destroyed by addition of iodine until I2 coloration persisted in organic layer. The latter was washed with 5% aqueous Na2S2O3, dried over Na2SO4 and evaporated. Purification of the crude product by flash column chromatography (heptane:ethyl acetate, 2:1) provides the title compound (5.19 g, 95%) as a light yellow oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07851463B2
Source datasetuspto-grants-2010_12
ORD IDord-ffdbad68405a45af8939b193f824dd85
Source noteuspto-grants-2010_12