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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1026163Generated: November 1, 2026

Allyl bromide → HCID 67179112, compound

https://huagongshe.com/reaction/1026163

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAllyl bromideHCID 7841—
ReactantSodium hydrideHCID 24758—
Reactant2-(4-Fluorophenyl)-2-propanolHCID 637733—
SolventTetrahydrofuranHCID 8028—
ProductHCID 67179112HCID 6717911260%

Reaction Steps

To a stirred solution of sodium hydride (1.47 g) in dry tetrahydrofuran (60 ml) was added dropwise under an argon atmosphere a solution of 2-(4-fluorophenyl)-2-propanol (4.35 g) in dry tetrahydrofuran (10 ml). The resulting yellow suspension was stirred at room temperature for 10 min. A solution of allyl bromide (3.1 ml) diluted in dry tetrahydrofuran (10 ml) was added slowly. The reaction mixture was stirred for 30 min and quenched by addition of water. The solution was extracted with ethyl acetate twice. The combined organic layers were dried (MgSO4) and evaporated. The crude product was purified by column chromatography (SiO2; gradient: heptane/EtOAc 100:0->90:10) to give 1-(1-allyloxy-1-methyl-ethyl)-4-fluoro-benzene (3.30 g, 60%) as a light yellow liquid. MS (EI): 179.0 ([M-CH3]).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08729113B2
Source datasetuspto-grants-2014_05
ORD IDord-21556bae6c604048976f3dc89be926d8
Source noteuspto-grants-2014_05