HuagongsheHuagongshe Chemistry Print Report · For research reference only
Dimethylamine → Methyl 2-benzyl-3-dimethylaminopropionate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Dimethylamine | HCID 674 | — |
| Reactant | Methyl 2-benzylprop-2-enoate | HCID 575761 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | Methyl 2-benzyl-3-dimethylaminopropionate | HCID 13653933 | — |
Reaction Steps
A solution of 30.0 g of methyl α-benzylacrylate, prepared by the method of R. B. Miller and B. F. Smith, Synth. Commun. 3, 359 (1973) in methanol (50 ml) is added to a solution of dimethylamine (71.0 g) in methanol (210 ml), and the mixture is stirred at room temperature for 48 hours. The solvent is removed under reduced pressure to give methyl 2-benzyl-3-dimethylaminopropionate as a yellow oil, used without purification in the next synthetic step; NMR: δ7.14 (s, 5H), 3.52 (s, 3H), 2.82 (m, 3H), 2.17 (s, 6H), 2.63-2.17 (m, remaining H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04588746 |
| Source dataset | uspto-grants-1986_05 |
| ORD ID | ord-6dafba882a5b449998cbf426826db1c7 |
| Source note | uspto-grants-1986_05 |