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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 430738Generated: October 30, 2026

Toluene → HCID 11448389, compound

https://huagongshe.com/reaction/430738

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTolueneHCID 1140—
ReactantSodium hydrideHCID 24758—
ReactantMethyl 3-methoxy-2-(2-methoxy-2-oxoethoxy)benzoateHCID 4141042—
ProductHCID 11448389HCID 1144838992%

Reaction Steps

Methyl 3-methoxy-2-(methoxycarbonylmethoxy)benzoate (19.39 g) was dissolved in toluene (200 ml). To this solution, sodium hydride (3.36 g) was added and the resultant was stirred at room temperature for 20 minutes, followed by refluxing the mixture for 2 hours. Toluene was evaporated off under reduced pressure and the residue was dissolved in DMF (150 ml). To this solution, acetic acid (2 ml) was added and the solvent was evaporated off under reduced pressure. The residue was dissolved in toluene (200 ml) and the solution was refluxed for 1 hour. The reaction solution was cooled to room temperature and poured into water (150 ml), followed by separating the organic layer. The aqueous layer was extracted with ethyl acetate (100 ml) and the organic layers were combined. The resultant was washed with saturated aqueous sodium hydrogen carbonate solution and with saturated brine, followed by drying the resultant over sodium sulfate. After removing sodium sulfate by filtration, the solvent was evaporated off, and the residue was purified by column chromatography (solvent: hexane/ethyl acetate=3/1) using silica gel to obtain the desire compound (18.42 g, yield: 92%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06323235B1
Source datasetuspto-grants-2001_11
ORD IDord-3f80aa0b6adb4d128d38fe2ab8487ebb
Source noteuspto-grants-2001_11