HuagongsheHuagongshe Chemistry Print Report · For research reference only
Cyclopentadiene → HCID 17861839, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Cyclopentadiene | HCID 7612 | — |
| Reactant | Allyl chloride | HCID 7850 | — |
| Reactant | Pivaloyl chloride | HCID 62493 | — |
| Reactant | Potassium tert-butoxide | HCID 23665647 | — |
| Product | HCID 12450215 | HCID 12450215 | — |
| Product | HCID 17861839 | HCID 17861839 | 10% |
Reaction Steps
5,5-Dimethyl-4-oxocaproaldehyde cl was prepared analogously to al by reaction of pivaloyl chloride and allyl chloride (see I.1.). 41 g (195 mmol) of c1 were reacted with cyclopentadiene and potassium tert-butylate and the mixture was worked up, analogously to instructions I.1. The reaction time was 19 hours at room temperature. Column chromatography gave 3.2 g (10%) of indene c2 as a yellow oil (2 double bond isomers).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05329033 |
| Source dataset | uspto-grants-1994_07 |
| ORD ID | ord-5888cfeb18e84b40b08e629d94086f6f |
| Source note | uspto-grants-1994_07 |