HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 863375Generated: October 26, 2026
2-(1,3-Dioxan-2-yl)ethyltriphenylphosphonium bromide → HCID 178509791, compound
https://huagongshe.com/reaction/863375
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 2-(1,3-Dioxan-2-yl)ethyltriphenylphosphonium bromide | HCID 2724168 | — |
| Reactant | Potassium tert-butoxide | HCID 23665647 | — |
| Reactant | HCID 178509803 | HCID 178509803 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 178509791 | HCID 178509791 | 91.6% |
Reaction Steps
A mixture of (2-(1,3-dioxan-2-yl)ethyl)triphenylphosphonium bromide (17.4 g, 38.0 millimols) with THF (100 ml) was cooled down to -20° C., followed by adding t-BuOK (4.5 g, 39.9 millimols) to the mixture, stirring for 30 minutes, dropwise adding to the mixture, a THF (35 ml) solution of trans-4-(4-cyanophenyl)cyclohexanecarbaldehyde (7.7 g, 36.1 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 3, to obtain raw 4-(trans-4-(3-(1,3-dioxan-2-yl) propenyl)cyclohexyl)benzonitrile (10.3 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-c669cc5417ba4fb298d038044be3122b |
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| Source note | uspto-grants-1998_02 |
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