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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1581821Generated: October 30, 2026

Water → Benzofuran-2,3-dione2-{o-[2-(tetrahydropyran-2-yloxy)-ethyl]-oxime}

https://huagongshe.com/reaction/1581821

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
Reactant2-(2-Bromoethoxy)tetrahydro-2H-pyranHCID 86621—
ReactantSodium MethoxideHCID 10942334—
ReactantHCID 178516824HCID 178516824—
SolventMethanolHCID 887—
ProductBenzofuran-2,3-dione2-{o-[2-(tetrahydropyran-2-yloxy)-ethyl]-oxime}HCID 5445679863.5%

Reaction Conditions

Temperature20 °C

Reaction Steps

5 g (0.03 mol) of benzofuran-2,3-dione 2-oxime (XI-1) are dissolved in 30 ml of methanol, and at 20° C. 15 ml of a 2 molar solution of sodium methoxide in methanol are added dropwise. The solvent is distilled off under reduced pressure. The crystalline residue is dissolved in 30 ml of N-methyl-2-pyrrolidinone and treated with 6.27 g (0.03 mol) of 2-(2-bromoethoxy)-tetrahydropyran at 20° C. The reaction mixture is stirred for 16 hours at 20° C., poured into 100 ml of water and the resulting mixture is extracted twice with 100 ml of dichloromethane each time. The solvent is distilled off under reduced pressure and the residue is chromatographed over silica gel using a mixture of diethyl ether/dichloromethane/petroleum ether (1:1:2). 5.55 g (62.1% of theory) of benzofuran-2,3-dione 2-{O-[2-(tetrahydropyran-2-yloxy)-ethyl]-oxime} (XIV-2) are obtained.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06730799B2
Source datasetuspto-grants-2004_05
ORD IDord-54176488babe4daeb1a5eb4299307638
Source noteuspto-grants-2004_05