HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1644735Generated: October 25, 2026
Sodium Acetate → 4-Acetoxy-6-fluoro-3-methyl-naphthalene-2-carboxylic acid methyl ester
https://huagongshe.com/reaction/1644735
Participants
| Role | Name | HCID | Charge |
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| Reactant | Sodium Acetate | HCID 517045 | — |
| Reactant | 2-(4-Fluoro-benzylidene)-3-methyl-succinic acid 1-methyl ester | HCID 66775587 | — |
| Solvent | Acetic Anhydride | HCID 7918 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | 4-Acetoxy-6-fluoro-3-methyl-naphthalene-2-carboxylic acid methyl ester | HCID 59350848 | 34% |
Reaction Steps
To a solution of crude 2-(4-fluoro-benzylidene)-3-methyl-succinic acid 1-methyl ester (approximately 49 g, 0.196 mol) in acetic anhydride (490 mL) was added sodium acetate (32.15 g, 0.392 mol) in one portion. The reaction mixture was stirred at 150° C. for 3 hours. After this time, the reaction mixture was cooled to room temperature, then stirred overnight. Acetic anhydride was removed in vacuo, providing a viscous brown oil. This crude product was dissolved in ethyl acetate. The resulting solution was washed with a saturated, aqueous ammonium chloride solution. The organic phase was dried over Na2SO4, filtered, and concentrated. Flash chromatography (Analogix SuperFlash™ 10% ethyl acetate in hexane) gave 18.4 g (34%) of 4-acetoxy-6-fluoro-3-methyl-naphthalene-2-carboxylic acid methyl ester as a yellow oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08124629B2 |
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| Source dataset | uspto-grants-2012_02 |
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| ORD ID | ord-17889a430be241ea8277e3a6dd473dbc |
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| Source note | uspto-grants-2012_02 |
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