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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2098947Generated: October 26, 2026

Sodium Iodide → 1-Bromo-3-cyclopropoxybenzene

https://huagongshe.com/reaction/2098947

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium IodideHCID 5238—
ReactantCesium carbonateHCID 10796—
Reactant3-BromophenolHCID 11563—
ReactantBromocyclopropaneHCID 78037—
SolventDimethylformamideHCID 6228—
SolventEthyl AcetateHCID 8857—
Product1-Bromo-3-cyclopropoxybenzeneHCID 5741695121%

Reaction Conditions

Temperature150 °C

Reaction Steps

To a solution of 3-bromophenol (0.57 g, 3.29 mmol) (commercially available from Aldrich) in dry DMF (5.0 mL) was added cyclopropyl bromide (0.53 mL, 6.62 mmol) (commercially available from Aldrich), sodium iodide (50.1 mg, 0.334 mmol), and cesium carbonate (3.2 g, 9.86 mmol). The reaction mixture was heated in a pressure tube to 150° C. After 19 hours, the reaction was cooled to room temperature then diluted with EtOAc, washed with water, and extracted three times with EtOAc. The combined organic layers were dried over sodium sulfate, filtered, and concentrated. The residue was purified by silica gel flash chromatography (0-5% EtOAc/hexane) to afford T24.1 as a colorless oil (144 mg, 21% yield). 1H NMR (400 MHz, CDCl3) δ ppm 7.29 (1H, m), 7.19 (2H, m), 6.99 (1H, d, J=7.8 Hz), 3.74 (1H, ddd, J=8.9, 5.8, 3.3 Hz), 0.81 (4H, ddd, J=11.2, 9.0, 8.8 Hz.).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08450522B2
Source datasetuspto-grants-2013_05
ORD IDord-f1727f421f1c4ba29d3ddb0891e5d64c
Source noteuspto-grants-2013_05