Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Ethanol | HCID 702 | — |
| Reactant | Sodium amide | HCID 24533 | — |
| Reactant | Cyclopropene | HCID 123173 | — |
| Reactant | 8-Iodooct-1-ene | HCID 13889810 | — |
| Solvent | Ammonia | HCID 222 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Product | 1-(Oct-7-enyl)-cyclopropene | HCID 22621655 | 67% |
Reaction Steps
A mixture of 0.43 g (11 mmol) of sodium amide in roughly 15 ml of ammonia was cooled to −78° C. A chilled solution of cyclopropene in ammonia (1:1, 0.85 g, 10 mmol) was poured into the reaction mixture. The reaction mixture was stirred at −78° C. for ½ hour, warmed briefly to the ammonia boiling point, then recooled to −78° C. 8-Iodooct-1-ene (1.2 g, 5 mmol) was added by syringe, and the reaction mixture was warmed to reflux for ½ hour. A few ml of ethanol were added. Ether (25 ml) was slowly added while the ammonia was allowed to distill out of the reaction mixture. The reaction mixture was washed with water, 0.5M HCl (2×), water and brine. It was dried over MgSO4, filtered and stripped. The product was purified by chromatography on silica gel using hexane as the eluent. A 10 mg sample of 67% pure 1-(oct-7-enyl)-cyclopropene was obtained.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06365549B2 |
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| Source dataset | uspto-grants-2002_04 |
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| ORD ID | ord-8c64df106f9d4203a153d539fb25673e |
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| Source note | uspto-grants-2002_04 |
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