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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2046930Generated: October 31, 2026

Potassium Carbonate → tert-butyl 3-(4-iodo-1H-pyrazol-1-yl)azetidine-1-carboxylate

https://huagongshe.com/reaction/2046930

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium CarbonateHCID 11430—
Reactant18-Crown-6HCID 28557—
Reactant4-IodopyrazoleHCID 77022—
ReactantTert-butyl 3-(methanesulfonyloxy)azetidine-1-carboxylateHCID 10753243—
SolventWaterHCID 962—
SolventDimethylformamideHCID 6228—
Producttert-butyl 3-(4-iodo-1H-pyrazol-1-yl)azetidine-1-carboxylateHCID 58431448—

Reaction Conditions

Temperature85 °C

Reaction Steps

A mixture of 3-methanesulfonyloxyazetidine-1-carboxylic acid tert-butyl ester (4.00 g, 15.9 mmol), 4-iodopyrazole (3.1 g, 15.9 mmol), potassium carbonate (2.85 g, 20.6 mmol) and 18-crown-6 (400 mg) in dry DMF (15 mL) was heated at 85° C. for 24 h. The reaction mixture was cooled to RT, poured into water and extracted with EtOAc (3×20 mL). The combined organic layers were washed with water (2×10 mL), dried over anhydrous sodium sulfate, filtered, and concentrated under reduced pressure. The residue was purified by column chromatography on silica gel eluting with hexanes/dichloromethane/ethyl acetate (8:1:1) to give the pure title compound. 1H NMR (300 MHz, CDCl3): δ=1.47 (s, 9H), 4.29 (m, 2H), 4.36 (m, 2H), 5.05 (m, 1H), 7.59 (s, 1H), 7.60 (s, 1H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08592448B2
Source datasetuspto-grants-2013_11
ORD IDord-62581956317d40479f94b5ea06259753
Source noteuspto-grants-2013_11