HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2201670Generated: October 29, 2026
Methacryloyl chloride → HCID 89880894, compound
https://huagongshe.com/reaction/2201670
Participants
| Role | Name | HCID | Charge |
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| Reactant | Methacryloyl chloride | HCID 13528 | — |
| Reactant | Benzeneethanamine, 4-nitro-, hydrochloride (1:1) | HCID 458983 | — |
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | HCID 89880894 | HCID 89880894 | — |
Reaction Steps
2-(4-Nitrophenyl)ethylamine hydrochloride (1.72 g) and sodium hydrogencarbonate (5.00 g) were dissolved in water (25 mL), to which ethyl acetate (25 mL) was added, followed by being stirred in an ice bath. Methacryloyl chloride (1.79 g) was added dropwise thereto. After stirring for 10 minutes, the organic layer was separated. The aqueous layer was extracted with ethyl acetate, the organic layers were combined, washed with water and brine, dried over anhydrous sodium sulfate, and evaporated under reduced pressure. The recrystallization was performed by using a mixture solvent of hexane and ethyl acetate. N-[2-(4-Nitrophenyl)ethyl]methacrylamide was obtained as pale yellowish crystals. The yield was 1.25 g (63%). Spectrum data of 1H-NMR (400 MHz, CDCl3) is shown for the obtained compound.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09365501B2 |
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| Source dataset | uspto-grants-2016_06 |
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| ORD ID | ord-a11db63021ac408ca32e6ee75de6c4b5 |
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| Source note | uspto-grants-2016_06 |
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