HuagongsheHuagongshe Chemistry Print Report · For research reference only
Imidazole → 3-O-(tert-Butyldimethylsilyl) Estrone
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Imidazole | HCID 795 | — |
| Reactant | Water | HCID 962 | — |
| Reactant | Estrone | HCID 5870 | — |
| Reactant | tert-Butyldimethylsilyl chloride | HCID 28928 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 3-O-(tert-Butyldimethylsilyl) Estrone | HCID 11811102 | 95% |
Reaction Steps
To a solution of estrone (100 g, 0.37 mole) in 400 ml of dichloromethane, imidazole (50.36 g, 0.74 mole) and t-butyl-dimethylsilyl chloride (61.3 g, 0.41 mole) were added. The solution was stirred at room temperature for 24 hours. Then water (200 ml) was added. The organic layer was partially evaporated and diisopropyl ether added. The white solid formed was collected by filtration and dried. It weighed 135.2 g, yield 95%, mp 172° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08987484B2 |
| Source dataset | uspto-grants-2015_03 |
| ORD ID | ord-f1e1a0adb26f4531bd6600ed6bd1ff28 |
| Source note | uspto-grants-2015_03 |