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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 238648Generated: October 30, 2026

Hydrochloric Acid → (3-Ethyl-6-fluoro-4-hydroxy-naphthalen-2-yl)-acetic acid methyl ester

https://huagongshe.com/reaction/238648

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantSodium MethoxideHCID 10942334—
Reactant(4-Acetoxy-3-ethyl-6-fluoro-naphthalen-2-yl)acetic acid methyl esterHCID 59326550—
SolventMethanolHCID 887—
Product(3-Ethyl-6-fluoro-4-hydroxy-naphthalen-2-yl)-acetic acid methyl esterHCID 5932649097.7%

Reaction Steps

A mixture of (4-acetoxy-3-ethyl-6-fluoro-naphthalen-2-yl)-acetic acid methyl ester (50 mg, 0.164 mmol), sodium methoxide (13 mg, 0.247 mmol), and methanol (4 mL) was stirred at room temperature for 2 hours. After the reaction mixture was acidified with concentrated hydrochloric acid to pH 5, a precipitate formed, which was then collected by filtration, and dissolved in ethyl acetate (20 mL). The organic solution was dried over sodium sulfate, and concentrated in vacuo to afford the crude product of (3-ethyl-6-fluoro-4-hydroxy-naphthalen-2-yl)-acetic acid methyl ester (42 mg, 97.7%) as a light yellow solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08642629B2
Source datasetuspto-grants-2014_02
ORD IDord-68472c4992bc455aa287b92fbbf72277
Source noteuspto-grants-2014_02