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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 604596Generated: October 25, 2026

Bromide ion → Benzene, 2-fluoro-4-methoxy-1-(1-methylethenyl)-

https://huagongshe.com/reaction/604596

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBromide ionHCID 259—
Reactant2'-Fluoro-4'-methoxyacetophenoneHCID 592821—
ReactantSodium bis(trimethylsilyl)amideHCID 2724254—
SolventTetrahydrofuranHCID 8028—
ProductBenzene, 2-fluoro-4-methoxy-1-(1-methylethenyl)-HCID 53363740—

Reaction Conditions

Temperature-78 °C

Reaction Steps

A solution of sodium bis(trimethylsilyl)-amide, 11.0M in tetrahydrofuran (714 mL, 0.714 mol) was added to a suspension of methyltriphenylphosphonum bromide (255 g, 0.714 mol) in THF (2.50 L) cooled with an ice bath. The resultant yellow colored suspension was stirred for 30 min at ice bath temperature and then cooled to −78° C. A solution of 2-fluoro-4-methoxyacetophenone (100 g, 0.595 mol) in THF (200 mL) was added dropwise and stirred at −78° C. for 1.5 h. The reaction mixture was allowed to warm to room temperature for one hour, quenched with acetic acid (˜80 mL) where color change was observed from yellow to off white and stirred for 30 min (pH ˜7)(slight exotherm noted). The mixture was concentrated to a slush, diluted with 7:2 hexane:EtOAc, and was allowed to sit overnight. Solids were removed by filtration and the filtrate was concentrated to yellow oil. The title compound was obtained after flash chromatography using 9:1 hexane:EtOAc as the eluant.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07910592B2
Source datasetuspto-grants-2011_03
ORD IDord-3d4646b20e6e485fbc3c949a27c57c16
Source noteuspto-grants-2011_03