HuagongsheHuagongshe Chemistry Print Report · For research reference only
Imidazole → 2-[2-[[(1,1-Dimethylethyl)dimethylsilyl]oxy]ethyl]furan
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Imidazole | HCID 795 | — |
| Reactant | Diethyl Ether | HCID 3283 | — |
| Reactant | tert-Butyldimethylsilyl chloride | HCID 28928 | — |
| Reactant | 2-Furanethanol | HCID 642110 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | 2-[2-[[(1,1-Dimethylethyl)dimethylsilyl]oxy]ethyl]furan | HCID 21875027 | 91.7% |
Reaction Steps
Imidazole (3.65 g, 53.6 mmol) and TBSCl (6.47 g, 42.9 mmol) were added to the solution of compound 255A (4.00 g, 35.7 mmol) in 50 mL of DMF. The mixture was stirred at rt for 2 h and then the reaction mixture was poured into ether. The ether solution was washed with water (1×), 1 N HCl (1×), water (1×) and brine (1×). The organic layer was dried over Na2SO4 and concentrated under reduced pressure. Purification by flash chromatography on silica gel eluting with 30% CH2Cl2/70% hexane gave 7.4 g (32.7 mmol, 91.7%) of 255B as a colorless oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06953679B2 |
| Source dataset | uspto-grants-2005_10 |
| ORD ID | ord-cc1cf2f1e8a54a23b55d533e242c27c1 |
| Source note | uspto-grants-2005_10 |