HuagongsheHuagongshe Chemistry Print Report · For research reference only
Dichloromethane → Chlorobutyl ferrocene
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Dichloromethane | HCID 6344 | — |
| Reactant | Trifluoroacetic acid | HCID 6422 | — |
| Reactant | Bis(eta-cyclopentadienyl) iron | HCID 7611 | — |
| Reactant | Sodium borohydride | HCID 4311764 | — |
| Product | Chlorobutyl ferrocene | HCID 15346559 | — |
Reaction Steps
A cold solution of freshly distilled trifluoroacetic acid (5 ml) was added to a solution of the ferrocene derivative, 1-Oxo-4-chlorobutylferrocene I, (5 g, 17.2 mmole) in dry dichloromethane (15 ml) at 0° C. Sodium borohydride (0.78 g) was added to the reaction mixture at 0° C. and the reaction mixture was stirred overnight at this temperature. After completion of the reaction as indicated from TLC, the reaction was quenched by adding water (50 ml) and the mixture was extracted with dichloromethane (2×25 ml).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08664417B2 |
| Source dataset | uspto-grants-2014_03 |
| ORD ID | ord-0e39a71419bc4a98ae9c36d74090bfde |
| Source note | uspto-grants-2014_03 |