HuagongsheHuagongshe Chemistry Print Report · For research reference only
Methacryloyl chloride → HCID 89880870, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Methacryloyl chloride | HCID 13528 | — |
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Reactant | 4-Nitrobenzylamine hydrochloride | HCID 11252467 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | HCID 89880870 | HCID 89880870 | — |
Reaction Steps
4-Nitrobenzylamine hydrochloride (1.51 g) and sodium hydrogencarbonate (4.13 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 (1.26 g) was added dropwise thereto. After stirring for 10 minutes, the mixture was extracted with ethyl acetate. After washing with water and brine, the organic layer was dried over anhydrous sodium sulfate and evaporated. After that, the recrystallization was performed by using a mixture solvent of hexane and ethyl acetate. N-(4-Nitrobenzyl)methacrylamide was obtained as pale yellowish crystals. The yield was 1.05 g (60%). Spectrum data of 1H-NMR (400 MHz, CDCl3) is shown for the obtained compound.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US09365501B2 |
| Source dataset | uspto-grants-2016_06 |
| ORD ID | ord-b00f862da8cb4ba0b9d3de9f64124d51 |
| Source note | uspto-grants-2016_06 |