HuagongsheHuagongshe Chemistry Print Report · For research reference only
1-Methylimidazole → HCID 86680637, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 1-Methylimidazole | HCID 1390 | — |
| Reactant | Tetrahydrofuran | HCID 8028 | — |
| Reactant | Bromodiphenylmethane | HCID 236603 | — |
| Reactant | 2-(pyridin-2-ylamino)ethanol | HCID 420844 | — |
| Product | HCID 86680637 | HCID 86680637 | 62% |
Reaction Steps
Diphenylmethyl bromide (0.1 mol; 24.75 g) was dissolved in 25 ml of tetrahydrofuran and placed in a flask together with N-pyridylethanolamine (0.05 mole-6.9 g) and 0.5 ml of catalytic N-methylimidazol, and then left for 72 hours in a dryer at temperature of 65° C. The product of this reaction was purified on a column filled with silica gel 60 of a particle size 70-230 mesh. Methanol gradient in methylene chloride was used as an eluting phase. Then the fractions containing the product of the reaction (N-pyridyl-N-[diphenylmethyl]aminoethanol) were isolated and combined. The excess of solvent was evaporated. The compound was characterized by means of the 1HNMR and 13CNMR spectra, presented in FIG. 9. 19.03 g were obtained (a yield of 62%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08759509B2 |
| Source dataset | uspto-grants-2014_06 |
| ORD ID | ord-567c8ac76e724cb2a89b253a585c5d1f |
| Source note | uspto-grants-2014_06 |