HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 436345Generated: October 25, 2026
Bicyclo[3.1.0]hexan-2-ol → HCID 131710021, compound
https://huagongshe.com/reaction/436345
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Bicyclo[3.1.0]hexan-2-ol | HCID 276343 | — |
| Reactant | Phosphonium, hexyltriphenyl-, bromide (1:1) | HCID 2724569 | — |
| Reactant | Bicyclo[3.1.0]hexan-3-ol | HCID 12724622 | — |
| Reactant | Butyllithium | HCID 178418339 | — |
| Solvent | Benzene | HCID 241 | — |
| Solvent | Hexane | HCID 8058 | — |
| Product | HCID 131710021 | HCID 131710021 | — |
Reaction Steps
A mixture of hexyltriphenylphosphonium bromide (102 g.) and benzene (1200 ml.) is stirred under nitrogen during addition of a solution of butyl lithium in hexane (146 ml. of a 15% solution - w/v). The resulting mixture is stirred 30 minutes. Then a solution of the mixture (27 g.) of products obtained according to Preparation 4 in 300 ml. of benzene is added dropwise with stirring during 30 minutes. The mixture is heated and stirred at 70° C. for 2.5 hours, and then is cooled to 25° C. The resulting precipitate is collected by filtration and washed with benzene. The filtrate and benzene wash are combined, washed with water, dried, and evaporated to give 58 g. of a mixture of the tetrahydropyranyl ethers of endo-6-(cis- and trans-1-heptenyl)bicyclo[3.1.0]hexan-3-ol and endo-6-(cis- and trans-1-heptenyl)bicyclo[3.1.0]hexan-2-ol.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04008263 |
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| Source dataset | uspto-grants-1977_02 |
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| ORD ID | ord-b154fc446dcb4e3ea497f6803f4b0908 |
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| Source note | uspto-grants-1977_02 |
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