Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Lithium aluminum hydride | HCID 28112 | — |
| Reactant | HCID 69250590 | HCID 69250590 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Product | HCID 85958219 | HCID 85958219 | — |
Reaction Steps
A suspension of 55.1 g (0.1 mol) of 5-bromo-1,2,3,4-tetraphenyl-5-p-vinylphenylcyclopenta-1,3-diene in 300 ml of ether was added in portions to a suspension of 11.5 g (0.3 mol) of Li[AlH4] in 150 ml of ether with stirring. The slightly yellow-brown suspension formed was refluxed for 2 hours to complete the reduction. After cooling to room temperature, excess Li[AlH4] was hydrolyzed first with ice water (caution: vigorous H2 evolution) and then with dilute hydrochloric acid. All volatile organic components were then distilled off from the reaction mixture using a rotary evaporator. The slightly yellow crude product was filtered off with suction and washed several times with water. For further purification, it was dried azeotropically with toluene, filtered and recrystallized (yield: 39.65 g (84%); found: C, 94.09%, H, 5.81%. calculated: C, 94.03%, H, 5.97%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07417247B2 |
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| Source dataset | uspto-grants-2008_08 |
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| ORD ID | ord-c41e926d033647f7904c7fad8eaa4b8d |
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| Source note | uspto-grants-2008_08 |
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