HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 863377Generated: October 30, 2026
(3-Fluoropropyl)triphenylphosphonium bromide → HCID 178444499, compound
https://huagongshe.com/reaction/863377
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | (3-Fluoropropyl)triphenylphosphonium bromide | HCID 11429580 | — |
| Reactant | Potassium tert-butoxide | HCID 23665647 | — |
| Reactant | HCID 178444507 | HCID 178444507 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 178444499 | HCID 178444499 | 87.8% |
Reaction Steps
A mixture of (3-fluoropropyl)triphenylphosphonium bromide (6.9 g, 17.1 millimols) with THF (40 ml) was cooled down to -20° C., followed by adding t-BuOK (1.9 g, 17.1 millimols) to the mixture, stirring the mixture for 30 minutes, dropwise adding to the mixture, a THF (30 ml) solution of trans-4-(trans-4-pentylcyclohexyl)cyclohexanecarbaldehyde (4.1 g, 15.5 millimols) so as to keep the temperature at -20° C., stirring the mixture at the same temperature for 2 hours, and treating the reaction product in the same manner as in Example 1, except that the quantity of ethyl acetate used for extraction was made 150 ml, to obtain raw trans-(trans-4-(4-fluorobutenyl)cyclohexyl)-4-pentylcyclohexane (4.2 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-153282506a144b27a4782ff732c7f6f3 |
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| Source note | uspto-grants-1998_02 |
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