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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1994517Generated: October 30, 2026

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

https://huagongshe.com/reaction/1994517

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, 1.0M in tetrahydrofuran (714 ml, 0.714 m) was added to a suspension of methyltriphenylphosphonum bromide (255 g, 0.714 m) in THF (2.50 L) cooled with an ice bath. The resultant yellow colored suspension was stirred for 30 minutes at ice bath temperature and then cooled to −78° C. A total of 2-fluoro-4-methoxyacetophenone (10 g, 0.595 m) in THF (200 ml) was added dropwise and stirred at −78° C. for 1.5 hours. 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 minutes (pH˜7)(slight exotherm noted). The mixture was concentrated to a slush, diluted with 7:2 hexane:ethyl acetate, 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 column using 9:1 hexane:ethyl as the eluant.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07652049B2
Source datasetuspto-grants-2010_01
ORD IDord-83d242eb53ed4a0fbeeb80c147a60ae4
Source noteuspto-grants-2010_01