HuagongsheHuagongshe Chemistry Print Report · For research reference only
Acetone → 3-Benzyl-2,2-dimethylimidazolidin-4-one
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Acetone | HCID 180 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | 2-amino-N-benzylacetamide | HCID 11126610 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | 3-Benzyl-2,2-dimethylimidazolidin-4-one | HCID 57433089 | — |
Reaction Steps
To a solution of N1-benzylglycinamide (3.00 g, 14.95 mmol) in MeOH (25 mL) were added acetone (5.50 mL, 74.75 mmol) and triethylamine (1.67 mL, 11.96 mmol). The solution was stirred and heated to reflux overnight under an atmosphere of nitrogen. The solvent was removed in vacuo, and the resulting orange oil was purified by flash column chromatography on silica gel using a gradient elution of 0-7% (MeOH/NH3)/CH2Cl2. Collection and concentration of the appropriate fractions afforded the product as a yellow oil. 1H NMR (400 MHz, CDCl3) δ 7.31-7.27 (m, 5H), 4.44 (s, 2H), 3.55 (s, 2H), 1.26 (s, 6H); ES MS (M+1)=205.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08003653B2 |
| Source dataset | uspto-grants-2011_08 |
| ORD ID | ord-e484d7d6f494408c9a853a58e8b6a794 |
| Source note | uspto-grants-2011_08 |