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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 244952Generated: October 30, 2026

Ethyl 3-(dimethylamino)-2-(4-hexylphenyl)acrylate → HCID 178442351, compound

https://huagongshe.com/reaction/244952

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl 3-(dimethylamino)-2-(4-hexylphenyl)acrylateHCID 86697470—
ReactantTert-butyl 2-(2-methyl-1-(p-tolyl)propan-2-yl)hydrazinecarboxylateHCID 86697472—
SolventAcetic AcidHCID 176—
SolventDiethyl EtherHCID 3283—
ProductHCID 178442351HCID 178442351—

Reaction Conditions

Temperature90 °C

Reaction Steps

Ethyl 3-(dimethylamino)-2-(4-hexylphenyl)acrylate and 0.50 g (1.8 mmol) of tert-butyl 2-(2-methyl-1-(p-tolyl)propan-2-yl)hydrazinecarboxylate were dissolved in 2 mL of acetic acid and stirred at 90° C. for 24 hours. After the stirring, the reaction mixture was mixed with 0.5 mL of acetic acid and stirred for 48 hours. After completion of the reaction, the reaction mixture was cooled to room temperature, diluted with diethyl ether and washed with distilled water, with saturated aqueous sodium hydrogen carbonate and with saturated aqueous sodium chloride successively. The organic layer was dried over anhydrous sodium sulfate and filtered, and the filtrate was concentrated under reduced pressure. The resulting residue was purified by intermediate pressure silica gel column chromatography (silica gel 30 g, ethyl acetate:hexane=0:100 to 35:65). The resulting solid was washed with isopropyl ether to give 164 mg of the desired product as a white solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08658686B2
Source datasetuspto-grants-2014_02
ORD IDord-7894eb2ebe044972a9dd513290bbc7e4
Source noteuspto-grants-2014_02