Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2363817Generated: October 26, 2026

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

https://huagongshe.com/reaction/2363817

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 light yellow solid. MS cald. for C13H12FO3 [(M+H)+] 235, obsd. 235.2.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08691993B2
Source datasetuspto-grants-2014_04
ORD IDord-4fbcde60047147ebbb2cb5df02afedbc
Source noteuspto-grants-2014_04