HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ethyl ketone → 3-Tert-butyl-6,6-diethylfulvene
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ethyl ketone | HCID 7288 | — |
| Reactant | Hexane | HCID 8058 | — |
| Reactant | Tert-butylcyclopentadiene | HCID 633714 | — |
| Reactant | Butyllithium | HCID 178418339 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 3-Tert-butyl-6,6-diethylfulvene | HCID 17818143 | 63% |
Reaction Steps
To a THF solution of 1.53 g (13 mmol) of tert-butylcyclopentadiene, 9.0 ml (14 mmol) of a hexane solution of n-butyllithium was dropwise added in a nitrogen atmosphere with ice cooling, followed by stirring at room temperature for one night. Then, 1.7 ml (16 mmol) of 3-pentanone was further added at −78° C., followed by stirring at room temperature for 2 days. To the reaction solution, water was added. The mixture was subjected to extraction with ether, then the solvent was distilled off, and the residue was subjected to column chromatography (silica gel, developing solvent: hexane) to obtain 1.50 g of a yellow liquid (Yield: 63%). The analyzed values are given below.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06939928B1 |
| Source dataset | uspto-grants-2005_09 |
| ORD ID | ord-a81a4da4746e46b48096f9970fccbf4f |
| Source note | uspto-grants-2005_09 |