HuagongsheHuagongshe Chemistry Print Report · For research reference only
Benzylamine → N-benzyl(2,2-dimethyl-1,3-dioxan-5-yl)methanamine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Benzylamine | HCID 7504 | — |
| Reactant | (2,2-Dimethyl-1,3-dioxan-5-yl)methyl methanesulfonate | HCID 10998661 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | N-benzyl(2,2-dimethyl-1,3-dioxan-5-yl)methanamine | HCID 25223589 | 85% |
Reaction Steps
A solution of (2,2-dimethyl-1,3-dioxan-5-yl)methyl methanesulfonate (1.70 g, 7.58 mmol) in benzylamine (10 mL, 92 mmol) was stirred at 80° C. and monitored by TLC. After 2 h the reaction was complete therefore concentrated in vacuo. The residue was diluted with toluene (containing a small amount of ethyl acetate) and washed with water, dried and concentrate in vacuo. Column chromatography on silica eluting with ethyl acetate afforded N-benzyl(2,2-dimethyl-1,3-dioxan-5-yl)methanamine (1.51 g, 85% yield) as a yellow oil. 13C NMR (CD3OD) δ 140.8, 129.4 (2XCH), 128.1, 99.3, 64.0 (2XCH2), 54.7, 33.7, 25.6, 23.0
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08853224B2 |
| Source dataset | uspto-grants-2014_10 |
| ORD ID | ord-381e66c3d44e480c8b3aaf16c69869b2 |
| Source note | uspto-grants-2014_10 |