HuagongsheHuagongshe Chemistry Print Report · For research reference only
Imidazole → N-cyclopentyl-O-tert-butyldimethylsilylhydroxylamine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Imidazole | HCID 795 | — |
| Reactant | N-cyclopentylhydroxylamine | HCID 10219393 | — |
| Reactant | Tert-butylmethylsilyl chloride | HCID 102463549 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Solvent | Hexane | HCID 8058 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | N-cyclopentyl-O-tert-butyldimethylsilylhydroxylamine | HCID 22385752 | 52.1% |
Reaction Steps
Imidazole (882 mg) and tert-butylmethylsilyl chloride (903 mg) were added to N-cyclopentylhydroxylamine (650 mg, 6.43 mmol) in dimethylformamide (10 ml). The mixture was stirred at room temperature for 3 hours. After diluting the mixture with ethyl acetate and hexane, the organic layer was washed with water and saturated aqueous sodium chloride. The organic layer was dried over magnesium sulfate, filtered, and concentrated in vacuo. The residue was purified by silica gel chromatography (hexane-ethyl acetate, 20:1 to 10:1) to give the title compound (722 mg) as a colorless oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06914062B2 |
| Source dataset | uspto-grants-2005_07 |
| ORD ID | ord-84347f0dee2743adbbf6297953be81fb |
| Source note | uspto-grants-2005_07 |