Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 238640Generated: October 30, 2026

Acetic Anhydride → (4-Acetoxy-6-fluoro-3-iodo-naphthalen-2-yl)acetic acid methyl ester

https://huagongshe.com/reaction/238640

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AnhydrideHCID 7918—
Reactant(6-Fluoro-4-hydroxy-3-iodo-naphthalen-2-yl)-acetic acid methyl esterHCID 59326608—
Catalyst4-(Dimethylamino)pyridineHCID 14284—
SolventHydrochloric AcidHCID 313—
SolventPyridineHCID 1049—
Product(4-Acetoxy-6-fluoro-3-iodo-naphthalen-2-yl)acetic acid methyl esterHCID 5932660053.3%

Reaction Steps

To a stirred solution of (6-fluoro-4-hydroxy-3-iodo-naphthalen-2-yl)-acetic acid methyl ester (500 mg, 1.4 mmol) and 4-dimethylaminopyridine (34 mg, 0.28 mmol) in pyridine (3 mL) was added acetic anhydride (160 μL, 1.7 mmol). After being stirred at room temperature overnight, the resulting mixture was diluted with 10% hydrochloric acid (20 mL), and extracted with ethyl acetate (30 mL×2). The combined organic layers were washed with brine (30 mL×2), dried over sodium sulfate, and concentrated in vacuo. The residue was purified by flash column (elution with 20% ethyl acetate in petroleum ether) to afford (4-acetoxy-6-fluoro-3-iodo-naphthalen-2-yl)acetic acid methyl ester (300 mg, 53%) as a white solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08642629B2
Source datasetuspto-grants-2014_02
ORD IDord-e7e184dd6ee14ab4acf86753c795b498
Source noteuspto-grants-2014_02