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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1363155Generated: November 3, 2026

Allyl bromide → 2-(Allyloxymethyl)-1-fluoro-3-iodobenzene

https://huagongshe.com/reaction/1363155

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAllyl bromideHCID 7841—
ReactantSodium hydrideHCID 24758—
Reactant(2-Fluoro-6-iodophenyl)methanolHCID 59705003—
SolventTetrahydrofuranHCID 8028—
Product2-(Allyloxymethyl)-1-fluoro-3-iodobenzeneHCID 59705016—

Reaction Steps

To a solution of (2-fluoro-6-iodophenyl)methanol (10 mmol) in 50 mL of THF was added NaH (12 mmol) in small portions at room temperature. After the addition, allylbromide (12 mmol) was added slowly via syringe. The reaction mixture was stirred 16 hours at room temperature. The resulting white heterogeneous mixture was quenched with water and then diluted with 100 mL of Et2O, followed by washing with water and brine. The organic layer was dried over MgSO4 and then concentrated to dryness in vacuo to offer 2.8 g of the title compound.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07884109B2
Source datasetuspto-grants-2011_02
ORD IDord-2f2efadf26944589a7d9958c1dac0d17
Source noteuspto-grants-2011_02