Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Ethylamine | HCID 6341 | — |
| Reactant | Methyl Acrylate | HCID 7294 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | Methyl N-ethyl-beta-alaninate | HCID 76973 | 30.3% |
Reaction Steps
Methyl acrylate (5.22 g, 60.6 mmol) is dissolved in methanol (20 mL) and cooled to −20° C. Ethylamine (2 M in tetrahydrofuran, 47 mL, 94 mmol) is added via addition funnel and the reaction is allowed to stir at −20° C. for 2 hours. Solvents were then removed in vacuo and the residue is distilled under reduced pressure to afford the title compound as a colorless liquid (2.41 g, 30% yield). 1H NMR (CDCl3) 1.11 (t, 3H, J=7.02 Hz), 2.53 (t, 2H, J=6.58 Hz), 2.66 (q, 2H, J=7.02 Hz), 2.89 (t, 2H, J=6.58 Hz), 3.69 (s, 3H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08362063B2 |
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| Source dataset | uspto-grants-2013_01 |
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| ORD ID | ord-763e89253a5846439d85d72ba124a2f8 |
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| Source note | uspto-grants-2013_01 |
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