HuagongsheHuagongshe Chemistry Print Report · For research reference only
Benzyl Bromide → 1-benzylimidazole-4-carbaldehyde
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Benzyl Bromide | HCID 7498 | — |
| Reactant | Sodium Carbonate | HCID 10340 | — |
| Reactant | 1H-imidazole-2-carbaldehyde | HCID 24955 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | 1-benzylimidazole-4-carbaldehyde | HCID 11095311 | 58.9% |
Reaction Conditions
| Temperature | 100 °C |
|---|
Reaction Steps
To a solution of imidazolecarboxaldehyde (1.0 g, 10.4 mmol) in DMF (10 mL) was added sodium carbonate (2.2 g, 20.8 mmol). The mixture was then treated with a solution of benzyl bromide (1.77 g, 10.4 mmol) in DMF (5 mL) dropwise and stirred for 1 h at 100° C. The reaction mixture was partitioned between EtOAc and water, and the aqueous layer was extracted with EtOAc. The organic layers were combined, dried with MgSO4, filtered, and concentrated to yield a dark brown oil (1.14 g). (m/z): [M+H]+calcd for C11H10N2O 187.21; found, 187.3. 1H NMR (d6-DMSO, 400 MHz) δ (ppm): 9.67 (s, 1H), 8.22, 8.08, 7.96, 7.90 (4 sets of singlets, total 2H), 7.30-7.24 (m, 5H), 5.49 (s, 1H), 5.25 (s, 1H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08211894B2 |
| Source dataset | uspto-grants-2012_07 |
| ORD ID | ord-fa614144e6ae40728899606b97906da2 |
| Source note | uspto-grants-2012_07 |