HuagongsheHuagongshe Chemistry Print Report · For research reference only
Dimethylformamide → 1,1'-Dimethyl-1H,1'H-2,2'-biimidazole
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Dimethylformamide | HCID 6228 | — |
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | Benzenesulfonic acid, 2-methyl-, methyl ester | HCID 90076 | — |
| Reactant | 2,2'-Biimidazole | HCID 101463 | — |
| Product | 1,1'-Dimethyl-1H,1'H-2,2'-biimidazole | HCID 10123778 | 80% |
Reaction Conditions
| Temperature | 0 °C |
|---|
Reaction Steps
To a stirred solution of 2,2′-biimidazole (Fieselmann, B. F., et al. Inorg. Chem. 17, 2078 (1978)) (4.6 g, 34.3 mmoles) in 100 mL dry DMF in a 250 ml round bottom flask cooled in an ice/water bath was added in portions NaH(60% in mineral oil, 2.7 g, 68.6 mmoles). After the solution was stirred at 0° C. for one hour under N2, methyl toluenesulfonate (10.3 mL, 68.6 mmoles) was added in small portions using a syringe over 30 min. The stirring of the solution in the ice/water bath was continued for 1 h and then at room temperature for 3 h. The solvent was removed by vacuum distillation. The dark residue was triturated with ether and then suction filtered and dried under vacuum. The product was purified by sublimation. Yield: 80%.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08092662B2 |
| Source dataset | uspto-grants-2012_01 |
| ORD ID | ord-d16489959e2340bc9f3fe64da65c777c |
| Source note | uspto-grants-2012_01 |