HuagongsheHuagongshe Chemistry Print Report · For research reference only
Pyridine → (r)-1-Ferrocenylethyl acetate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Pyridine | HCID 1049 | — |
| Reactant | Acetic Anhydride | HCID 7918 | — |
| Reactant | HCID 178462227 | HCID 178462227 | — |
| Product | (r)-1-Ferrocenylethyl acetate | HCID 15328554 | — |
Reaction Steps
500 g (6.32 mol) of pyridine and subsequently 600 g (5.88 mol) of acetic anhydride were added dropwise while stirring to the crude (R)-(1-hydroxyethyl) ferrocene from Example 1 at 25° C. under argon. The reaction mixture was allowed to stand for a further 20 hours at 25° C., then hydrolysed with 1.5 l of ammonium chloride solution (20%) and extracted three times with 1.5 l each time of ethyl acetate. The solvent was distilled off from the combined organic phases.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05760264 |
| Source dataset | uspto-grants-1998_06 |
| ORD ID | ord-6c2d14aa28c440a2b675cefd54eb7222 |
| Source note | uspto-grants-1998_06 |