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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 348414Generated: November 1, 2026

Potassium Iodide → Tert-butyl 3-iodoazetidine-1-carboxylate

https://huagongshe.com/reaction/348414

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium IodideHCID 4875—
ReactantTert-butyl 3-(methanesulfonyloxy)azetidine-1-carboxylateHCID 10753243—
SolventDimethylformamideHCID 6228—
ProductTert-butyl 3-iodoazetidine-1-carboxylateHCID 11000522—

Reaction Conditions

Temperature100 °C

Reaction Steps

A mixture of tert-butyl 3-[(methylsulphonyl)oxy]-1-azetidinecarboxylate (Synlett; 1998; 379), (5.0 g, 19.9 mmol), and potassium iodide (16.5 g, 99.4 mmol) in N,N-dimethylformamide (25 ml), was heated at 100° C. for 42 hours. The cooled mixture was partitioned between water and ethyl acetate, and the layers separated. The organic phase was dried (MgSO4), concentrated under reduced pressure and the residue azeotroped with xylene. The crude product was purified by column chromatography on silica gel using dichloromethane as eluant, to give the title compound, 3.26 g.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07176311B2
Source datasetuspto-grants-2007_02
ORD IDord-2e629d92b8ac4abb96244ce52487c413
Source noteuspto-grants-2007_02