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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1468326Generated: October 26, 2026

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

https://huagongshe.com/reaction/1468326

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSulfuric AcidHCID 1118—
ReactantEthyl acetate hexaneHCID 21226206—
Reactant6-Fluoro-4-hydroxy-3-methyl-naphthalene-2-carboxylic acidHCID 86683825—
SolventMethanolHCID 887—
Product6-Fluoro-4-hydroxy-3-methyl-naphthalene-2-carboxylic acid methyl esterHCID 5932657354%

Reaction Steps

To a 0° C. solution of crude 6-fluoro-4-hydroxy-3-methyl-naphthalene-2-carboxylic acid (28 g, approx. 118 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, 54%) as a light yellow solid. MS calcd. for C13H12FO3 [(M+H)+] 235, obsd. 235.2.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09000044B2
Source datasetuspto-grants-2015_04
ORD IDord-1a473be64f3d47f8897035e553d4f38a
Source noteuspto-grants-2015_04