HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 840078Generated: October 31, 2026
HCID 22621682, compound → HCID 22621659, compound
https://huagongshe.com/reaction/840078
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | HCID 22621682 | HCID 22621682 | — |
| Reactant | HCID 22621695 | HCID 22621695 | — |
| Reactant | Potassium tert-butoxide | HCID 23665647 | — |
| Solvent | Dimethyl Sulfoxide | HCID 679 | — |
| Product | HCID 22621659 | HCID 22621659 | — |
Reaction Steps
To a solution of 1.90 g of an equal mixture of 2-bromo-1,1-dipentyl-cyclopropane and 1,1-dipentyl-cyclopropane in 10 ml dimethylsulfoxide was added 0.818 g (0.00308 mol) of potassium t-butoxide. The resulting mixture was heated to 85° C. for 5 hours and then stirred at room temperature for 16 hours. To this was added 0.100 g of potassium t-butoxide. The resulting mixture was heated to 85° C. for 2 hours then cooled to room temperature. The reaction mixture was poured onto water and then extracted with diethyl ether. The resulting mixture was transferred to a separatory funnel and the phases were separated. The organic layer was dried over MgSO4 and filtered. The solvent was removed from the filtrate in vacuo to yield 1.90 g of 3,3-dipentyl-cyclopropene mixed in equal parts with 1,1-dipentyl-cyclopropane as an oil.
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-4ce06228bd824381a5382d778ff8f332 |
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| Source note | uspto-grants-2002_04 |
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