HuagongsheHuagongshe Chemistry Print Report · For research reference only
1-Methylimidazole → 1-Methyl-5-(tri-n-butylstannyl)imidazole
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 1-Methylimidazole | HCID 1390 | — |
| Reactant | N,N,N',N'-Tetramethylethylenediamine | HCID 8037 | — |
| Reactant | Tributyltin Chloride | HCID 15096 | — |
| Reactant | Butyllithium | HCID 178418339 | — |
| Product | 1-Methyl-5-(tri-n-butylstannyl)imidazole | HCID 10915651 | 8.8% |
Reaction Steps
Butyllithium (3.75 mL, 9.40 mmol) and TMEDA (2.24 mL, 14.85 mmol) were stirred at −20° C. in hexanes (7 mL) in an ethanol/dry ice/water bath for 30 minutes. 1-Methylimidazole (0.5 mL, 6.27 mmol) was added and the mixture stirred at room temperature for 1 h. After cooling to −20° C., Bu3SnCl (1.70 mL, 15.67 mmol) was added dropwise. The reaction stirred for 15 minutes at −20° C. then at room temperature overnight before being quenched with 1:1 EtOAc/water (20 mL). The layers were separated and the aqueous layer extracted with EtOAc (3×). The combined organics were washed with water, dried over Na2SO4, concentrated, and chromatographed (4:96 MeOH/EtOAc) to give 1-methyl-5-tributylstannanyl-1H-imidazole (0.486 g).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07214802B2 |
| Source dataset | uspto-grants-2007_05 |
| ORD ID | ord-bfb644dcc1d04a6aba5a85f2c3c45c81 |
| Source note | uspto-grants-2007_05 |