HuagongsheHuagongshe Chemistry Print Report · For research reference only
Acetonitrile → dimethyl[benzyl(methyl)amino]propanedioate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Acetonitrile | HCID 6342 | — |
| Reactant | N-Methylbenzylamine | HCID 7669 | — |
| Reactant | Dimethyl bromomalonate | HCID 70087 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | dimethyl[benzyl(methyl)amino]propanedioate | HCID 222087 | 96% |
Reaction Steps
To an acetonitrile (60 mL) solution of N-methylbenzylamine (15 mL), an acetonitrile (10 mL) solution of dimethyl bromomalonate (12 g) was added dropwise at room temperature, and the mixture was stirred for 6 hours at room temperature. Toluene (0.20 L) was added, insolubles were filtered off, and the filtrate was concentrated under reduced pressure. To the residue, toluene (0.10 L) and OH type silica gel (6.0 g) were added, and the mixture was stirred for 20 minutes at room temperature and then filtered. The filtrate was concentrated under reduced pressure to obtain dimethyl [benzyl(methyl)amino]propanedioate (pale yellow oil) (14 g, 96%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US09073821B2 |
| Source dataset | uspto-grants-2015_07 |
| ORD ID | ord-e76fa215d20c457098063545c4562b99 |
| Source note | uspto-grants-2015_07 |