HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1862068Generated: November 2, 2026
1,2-Dimethoxyethane → Bis(eta-cyclopentadienyl) iron
https://huagongshe.com/reaction/1862068
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 1,2-Dimethoxyethane | HCID 8071 | — |
| Reactant | Potassium tert-butoxide | HCID 23665647 | — |
| Reactant | HCID 178519520 | HCID 178519520 | — |
| Solvent | Water | HCID 962 | — |
| Product | Bis(eta-cyclopentadienyl) iron | HCID 7611 | 82.6% |
Reaction Steps
In a dry 2-L flask equipped with a mechanical stirrer and a reflux condenser topped with a nitrogen-inlet tube was charged with 1L of DME and 193 g (1.6 mol) of KOtBu. Under N2 atmosphere, 8.8 mL (0.48 mol) of water was added to the crude (2-chlorobenzoyl) ferrocene to give a red solution. The red solution was stirred and refluxed under N2. As the reaction proceeded with fade of color to tan. The reaction mixture was cooled and poured into 2 L of water. The resulting solution was washed with 2×400 mL of Et2O. The combine organic layer was extracted with 2×200 ml of 10% NaOH. The aqueous phase are then combined and acidified with concentrated HCl. The precipitate was collected by filtration and was dried in are to give yellow power 1 (76 g, 82.6%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US06534657B2 |
|---|
| Source dataset | uspto-grants-2003_03 |
|---|
| ORD ID | ord-b549f338c70c45edb343fc2d6dfc0b23 |
|---|
| Source note | uspto-grants-2003_03 |
|---|