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
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Bromide ion | HCID 259 | — |
| Reactant | 2'-Fluoro-4'-methoxyacetophenone | HCID 592821 | — |
| Reactant | Sodium bis(trimethylsilyl)amide | HCID 2724254 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | Benzene, 2-fluoro-4-methoxy-1-(1-methylethenyl)- | HCID 53363740 | — |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07652049B2 |
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| Source dataset | uspto-grants-2010_01 |
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| ORD ID | ord-83d242eb53ed4a0fbeeb80c147a60ae4 |
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| Source note | uspto-grants-2010_01 |
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