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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1028546Generated: October 28, 2026

2'-Fluoro-4'-methoxyacetophenone → Benzene, 2-fluoro-4-methoxy-1-(1-methylethenyl)-

https://huagongshe.com/reaction/1028546

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2'-Fluoro-4'-methoxyacetophenoneHCID 592821—
ReactantSodium bis(trimethylsilyl)amideHCID 2724254—
CatalystMethyltriphenyliphosphonium bromideHCID 74505—
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 methyltriphenylphosphonium 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 (100 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 numberUS08735435B2
Source datasetuspto-grants-2014_05
ORD IDord-834b1594bf9d436b92091c03d408e084
Source noteuspto-grants-2014_05