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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1361059Generated: October 30, 2026

Imidazole → 1-Fluoro-4-((4-iodobut-2-enyloxy)methyl)-2-methylbenzene

https://huagongshe.com/reaction/1361059

Reaction equation

Participants

RoleNameHCIDCharge
ReactantImidazoleHCID 795—
ReactantIodineHCID 807—
ReactantTriphenylphosphineHCID 11776—
ReactantSodium ThiosulfateHCID 24477—
Reactant4-(4-Fluoro-3-methylbenzyloxy)but-2-en-1-olHCID 66968450—
SolventDichloromethaneHCID 6344—
Product1-Fluoro-4-((4-iodobut-2-enyloxy)methyl)-2-methylbenzeneHCID 66968201—

Reaction Conditions

Temperature0 °C

Reaction Steps

To a solution of triphenylphosphine (2.6 g, 9.9 mmol) in anhydrous 40 mL DCM was added imidazole (1.4 mg, 20.4 mmol) and iodine (2.5 mg, 9.9 mmol) at 0° C. The reaction mixture was stirred for 30 min at 0° C. and then 4-(4-Fluoro-3-methylbenzyloxy)but-2-en-1-ol (1.3 g, 6.2 mmol) in 10 mL DCM was added to the mixture. The resulting mixture was stirred at 0° C. for 2 h and the temperature was slowly raised to room temp over a period of 2 h. 20 mL of 10% sodium thiosulfate was added and extracted with more DCM (3×30 mL). The combined DCM layer was washed with brine (2×30 mL) and dried over sodium sulfate. Evaporation of solvent left the crude product as an oil from which the product was isolated by Flash column chromatography eluting with 0% to 10% ethyl acetate/hexane to give the title compound, 1.5 g, as a light yellow oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07879911B2
Source datasetuspto-grants-2011_02
ORD IDord-bc79be4db39646f3a60a62890af4a380
Source noteuspto-grants-2011_02