HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 726834Generated: October 31, 2026
Acetic Acid → 5,5'-(Hexane-2,5-diylidene)di(cyclopenta-1,3-diene)
https://huagongshe.com/reaction/726834
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Acetic Acid | HCID 176 | — |
| Reactant | Cyclopentadiene | HCID 7612 | — |
| Reactant | 2,5-Hexanedione | HCID 8035 | — |
| Reactant | Pyrrolidine | HCID 31268 | — |
| Solvent | Methanol | HCID 887 | — |
| Solvent | Water | HCID 962 | — |
| Product | 5,5'-(Hexane-2,5-diylidene)di(cyclopenta-1,3-diene) | HCID 14951997 | — |
Reaction Steps
In a modified reaction procedure [a], 11.0 g (96.3 mmol) of 2,5-hexanedione and 12.7 g (193 mmol) of freshly cracked cyclopentadiene are dissolved in 60 ml of methanol, the solution is cooled to 0° C., and 8.60 g (121 mmol) of pyrrolidine are added. The reaction solution is stirred at 0° C. for 90 minutes, hydrolyzed using 5 ml of glacial acetic acid and 50 ml of water, and extracted twice with 70 ml of diethyl ether in each case, and the combined organic phases are washed with saturated sodium chloride solution and dried over magnesium sulfate, giving, after removal of the solvent in vacuo, 18.0 g (89%) of the difulvene as an orange-red, oily residue.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05710297 |
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| Source dataset | uspto-grants-1998_01 |
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| ORD ID | ord-06b1d13fa96741a394e6f958ea2a4e97 |
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| Source note | uspto-grants-1998_01 |
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