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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 520738Generated: October 30, 2026

Ethyl Acrylate → HCID 11300104, compound

https://huagongshe.com/reaction/520738

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl AcrylateHCID 8821—
ReactantSodium HydroxideHCID 14798—
ReactantDiphenylmethylidenehydrazineHCID 79304—
ReactantSodium ChloriteHCID 23668197—
ReactantHCID 88047892HCID 88047892—
SolventWaterHCID 962—
SolventDichloromethaneHCID 6344—
SolventBenzyldimethyloctylammonium chlorideHCID 13740—
ProductHCID 11300104HCID 1130010456%

Reaction Steps

Diphenylketone hydrazone (8.9 g, 45.4 mmol) in DCM (19 mL) was mixed with KI (0.45 g) in water (0.6 mL) and benzyldimethyloctylammonium chloride (10 mg). To the mixture was added the aqueous solution composing of 25% NaOH (27 mL), water (18 mL), and sodium chlorite (12-14%, 28 mL) at 5° C. with vigorous stirring. Twenty minutes later after addition, the stirring was turned off to let the reaction mixture separate. The red DCM solution was separated and dried over anhydrous Na2SO4. After removing the desiccant, the solvent was removed under reduced pressure; the residue was re-dissolved in hexane, and the unreacted hydrazone and side product was insoluble in hexane and removed by filtration. The red hexane diphenyl diazomethane solution was added to ethyl acrylate (13.6 g, 136 mmol) at 50° C. within 30 mints. When the red colour fade off the solvent and excess of ethyl acrylate was removed under reduced pressure to give crude product with 94% purity in 56-94% yield.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09328074B2
Source datasetuspto-grants-2016_05
ORD IDord-6e9c1437c5bc437d990c387f659c0efb
Source noteuspto-grants-2016_05