HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2261502Generated: October 25, 2026
Diethyl Ether → N-methacryloylasparagineamide
https://huagongshe.com/reaction/2261502
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Diethyl Ether | HCID 3283 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | Methacryloyl chloride | HCID 13528 | — |
| Reactant | (S)-2-Aminosuccinamide hydrochloride | HCID 16218940 | — |
| Solvent | Methanol | HCID 887 | — |
| Solvent | Water | HCID 962 | — |
| Product | N-methacryloylasparagineamide | HCID 86614806 | — |
Reaction Steps
A 11.3 ml portion of methacrylic acid chloride, 1 g of asparagineamide hydrochloride (mfd. by Kokusan Kagaku) and 50 ml of diethyl ether were put into a 300 ml capacity eggplant type flask and stirred on an ice bath. Next, 20 ml of saturated potassium carbonate aqueous solution was added dropwise thereto. Thereafter, this was stirred on an ice bath for 30 minutes and then at room temperature for 12 hours. Diethyl ether layer in the thus obtained reaction liquid was discarded, and the water layer was dissolved in 100 ml of methanol. After filtration, the filtrate was concentrated under a reduced pressure and fractionated by a silica gel column using methanol as the developing solvent. The thus obtained amide compound fraction was purified using an ion exchange resin (“Dynaion (trade name) PA 412” mfd. by Mitsubishi Kagaku) After concentration under a reduced pressure and subsequent drying under a reduced pressure, 0.43 g of colorless crystals were obtained.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07847047B2 |
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| Source dataset | uspto-grants-2010_12 |
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| ORD ID | ord-2b77fb6cdb414d78b7f09e69d2abd348 |
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| Source note | uspto-grants-2010_12 |
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