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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 225952Generated: October 25, 2026

Water → Ethyl 3-(1,3-dimethyl-1H-indol-2-yl)-5-ethyl-4,5-dihydro-5-isoxazole-carboxylate

https://huagongshe.com/reaction/225952

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantEthyl 2-methylidenebutanoateHCID 291416—
ReactantSodium HypochloriteHCID 23665760—
Reactant1,3-Dimethyl-1H-indol-2-aldehyde oximeHCID 85271892—
CatalystTriethylamineHCID 8471—
SolventDichloromethaneHCID 6344—
ProductEthyl 3-(1,3-dimethyl-1H-indol-2-yl)-5-ethyl-4,5-dihydro-5-isoxazole-carboxylateHCID 6883506335.3%

Reaction Steps

1,3-Dimethyl-1H-indol-2-aldehyde oxime derivative (356 mg, 2.07 mmol) was dissolved in dichloromethane (20 ml), and the mixture was kept at 0□. Ethyl 2-ethylacrylate (345 mg, 1.3 Eq) and triethylamine (6 drops) were dissolved in dichloromethane (5 ml), thus obtained solution was slowly added to the above, and sodium hypochlorite solution (5.5 ml) was further added. The reaction solution was warmed to room temperature and stirred for 4 hours. Water (20 ml) was added, and the mixture was extracted with dichloromethane (40 ml×2), washed with aqueous sodium chloride solution (20 ml), dried over magnesium sulfate, filtered, and concentrated under reduced pressure. The residue was purified by column chromatography (15% ethyl acetate-hexane) to give the title compound (230 mg, Yield 35%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07557133B2
Source datasetuspto-grants-2009_07
ORD IDord-427150645de04ad59bb5ae8c4cc2ae4b
Source noteuspto-grants-2009_07