HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ferroceneacetic acid → 1273-90-1
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ferroceneacetic acid | HCID 15768501 | — |
| Reactant | Aluminium lithium hydride | HCID 21226445 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Product | 1273-90-1 | HCID 15854803 | — |
Reaction Steps
2-ferrocenylethyl alcohol was synthesized by reducing ferrocenyl acetic acid with lithiumaluminum hydride. 1.4 g of LiAlH4 are placed in a flask containing ether and equipped with a soxhlet apparatus. Ferrocene acetic acid (0.9 g) is extracted by this apparatus for 48 hours. After cooling, the excess reagent is decomposed with water and the solution washed thoroughly with a solution of sodium bicarbonate, dried and evaporated to dryness. The residual oil is crystallized from hexane. It has a melting point of 41° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06171757B2 |
| Source dataset | uspto-grants-2001_01 |
| ORD ID | ord-11f98d20315046d3b418847405911c2b |
| Source note | uspto-grants-2001_01 |