HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 863373Generated: October 27, 2026
Tetrahydrofuran → HCID 178509749, compound
https://huagongshe.com/reaction/863373
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Tetrahydrofuran | HCID 8028 | — |
| Reactant | (3-Fluoropropyl)triphenylphosphonium bromide | HCID 11429580 | — |
| Reactant | Potassium tert-butoxide | HCID 23665647 | — |
| Reactant | HCID 178509750 | HCID 178509750 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | HCID 178509749 | HCID 178509749 | 90.4% |
Reaction Steps
A mixture of (3-fluoropropyl)triphenylphosphonium bromide (15.1 g, 37.4 millimols) with THF (70 ml) was cooled down to -20° C., followed by adding t-BuOK (4.2 g, 37.4 millimols) to the mixture, stirring for one hour, dropwise adding to the mixture, a THF (100 ml) solution of trans-4-(trans-4-(2-(4-cyanophenyl)ethyl)cyclohexyl)cyclohexanecarbaldehyde (11.0 g, 34.0 millimols) so as to keep the temperature at -20° C. or lower, stirring the mixture at the same temperature for 2 hours, and treating the reaction product in the same manner as in Example 2, except that the quantity of ethyl acetate was made 500 ml, to obtain raw 4-(2-(trans-4-(trans-4-(4-fluorobutenyl)cyclohexyl)cyclohexyl)ethyl)benzonitrile (11.3 g).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05720899 |
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| Source dataset | uspto-grants-1998_02 |
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| ORD ID | ord-25d75464911f438f994665cdf3ea59a7 |
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| Source note | uspto-grants-1998_02 |
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