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
Participants
| Role | Name | HCID | Charge |
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| Reactant | Ethyl 3-(dimethylamino)-2-(4-hexylphenyl)acrylate | HCID 86697470 | — |
| Reactant | Tert-butyl 2-(2-methyl-1-(p-tolyl)propan-2-yl)hydrazinecarboxylate | HCID 86697472 | — |
| Solvent | Acetic Acid | HCID 176 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Product | HCID 178442351 | HCID 178442351 | — |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08658686B2 |
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| Source dataset | uspto-grants-2014_02 |
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| ORD ID | ord-7894eb2ebe044972a9dd513290bbc7e4 |
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| Source note | uspto-grants-2014_02 |
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