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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1261426Erstellt: 27. Oktober 2026

Sulfuric Acid → 6-Fluoro-4-hydroxy-3-methyl-naphthalene-2-carboxylic acid methyl ester

https://huagongshe.com/reaction/1261426

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktSulfuric AcidHCID 1118—
EduktEthyl acetate hexaneHCID 21226206—
Edukt6-Fluoro-4-hydroxy-3-methyl-naphthalene-2-carboxylic acidHCID 86683825—
LösungsmittelMethanolHCID 887—
Produkt6-Fluoro-4-hydroxy-3-methyl-naphthalene-2-carboxylic acid methyl esterHCID 5932657350%

Reaktionsschritte

To a 0° C. solution of 6-fluoro-4-hydroxy-3-methyl-naphthalene-2-carboxylic acid (28 g, 127 mmol) in MeOH (240 mL) was added concentrated sulfuric acid (18.9 mL, 382 mmol) dropwise. The reaction mixture was then warmed to room temperature and refluxed overnight. After this time, the methanol was distilled off under reduced pressure, and the crude mixture was diluted with ethyl acetate. This solution was washed with saturated aqueous NaHCO3. The organic phase was dried over Na2SO4, filtered and concentrated under reduced pressure to give the crude product. Silica gel column chromatography (6% ethyl acetate-hexane) afforded 6-fluoro-4-hydroxy-3-methyl-naphthalene-2-carboxylic acid methyl ester (14.8 g, 50%) as light yellow solid. MS cald. for C13H12FO3 [(M+H)+]: 235, obsd. 235.2.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08470884B2
Quelldatensatzuspto-grants-2013_06
ORD IDord-24b670ed1b4344b583cc1430a3e25928
Quellennotizuspto-grants-2013_06