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
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Sulfuric Acid | HCID 1118 | — |
| Reactant | Ethyl acetate hexane | HCID 21226206 | — |
| Reactant | 6-Fluoro-4-hydroxy-3-methyl-naphthalene-2-carboxylic acid | HCID 86683825 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | 6-Fluoro-4-hydroxy-3-methyl-naphthalene-2-carboxylic acid methyl ester | HCID 59326573 | 54% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US08691993B2 |
|---|
| Source dataset | uspto-grants-2014_04 |
|---|
| ORD ID | ord-4fbcde60047147ebbb2cb5df02afedbc |
|---|
| Source note | uspto-grants-2014_04 |
|---|