HuagongsheHuagongshe Chemistry Print Report · For research reference only
Triethylamine → cyanomethyl 2-(N-methylpent-4-enamido)acetate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | 4-Pentenoyl chloride | HCID 4228493 | — |
| Reactant | Cyanomethyl 2-(methylamino)acetate hydrochloride | HCID 117736071 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | cyanomethyl 2-(N-methylpent-4-enamido)acetate | HCID 89668754 | 88.4% |
Reaction Steps
Cyanomethyl 2-(methylamino)acetate hydrochloride (Compound SP703) (3.00 g, 18.3 mmol) and triethylamine (6.34 ml, 45.5 mmol) were dissolved in dichloromethane (30 ml) under a nitrogen atmosphere, and pent-4-enoyl chloride (2.60 g, 22.0 mmol) was added dropwise at 0° C. The reaction solution was stirred at room temperature for 2 hours and 30 minutes and then concentrated under reduced pressure. The resulting residue was dissolved in ethyl acetate, and the solid was removed by filtration. The solution was concentrated under reduced pressure and purified by column chromatography (ethyl acetate:petroleum ether=1:10→2:7) to afford cyanomethyl 2-(N-methylpent-4-enamido)acetate (Compound SP704) (3.40 g, 88%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US09409952B2 |
| Source dataset | uspto-grants-2016_08 |
| ORD ID | ord-d6bfa8d7fc1d422b84a561755ca54dda |
| Source note | uspto-grants-2016_08 |