Zurück
HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 21351Erstellt: 25. Oktober 2026

Benzoic Acid → 3-Fluoro-4-methoxybenzoic acid

https://huagongshe.com/reaction/21351

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktBenzoic AcidHCID 243—
EduktSodium HydroxideHCID 14798—
EduktBromineHCID 24408—
Edukt1-(3-Fluoro-4-methoxyphenyl)ethan-1-oneHCID 96828—
EduktSodiumHCID 5360545—
Eduktsodium hypobromiteHCID 178507097—
LösungsmittelWaterHCID 962—
Lösungsmittel1,4-DioxaneHCID 31275—
Produkt3-Fluoro-4-methoxybenzoic acidHCID 2733401—
Produktsodium hypobromiteHCID 178507097—

Reaktionsschritte

3-fluoro-4-methoxyacetophenone (11.5 g) was dissolved in 100 ml dioxane and NaOBr solution (as prepared below) was added dropwise, with constant stirring with a stir bar at room temperature. The NaOBr solution was prepared by dissolving 40 g of NaOH in 500 ml of water, cooling to 0° C. in an ice bath, and adding bromine (12.5 ml) dropwise while stirring with stir bar; bromine was added slowly so that the reaction mixture did not exceed 5° C. After overnight stirring of the 3-fluoro-4-methoxyacetophenone, dioxane and NaOBr solution, the reaction mixture was diluted with water (200 ml). Since the reaction mixture was basic, the product, benzoic acid, was in water as its sodium salt. The resultant mixture was partitioned between ether and water. The ether layer was washed with dilute aqueous NaOH to extract any remaining product as Na salt. The aqueous layers were combined and acidified to pH 1 to precipitate the benzoic acid. The resulting acid was extracted with ether. The ether layer was washed with water a few times, dried with MgSO4, and filtered. Rotary evaporation of the ether fraction afforded 3-fluoro-4-methoxybenzoic acid (IV) in 85% yield.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS05422037
Quelldatensatzuspto-grants-1995_06
ORD IDord-93fc24620c104a2c9d3ba2a8256382e3
Quellennotizuspto-grants-1995_06