HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 863376Generated: October 25, 2026
2-(1,3-Dioxan-2-yl)ethyltriphenylphosphonium bromide → HCID 178509799, compound
https://huagongshe.com/reaction/863376
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 2-(1,3-Dioxan-2-yl)ethyltriphenylphosphonium bromide | HCID 2724168 | — |
| Reactant | Potassium tert-butoxide | HCID 23665647 | — |
| Reactant | HCID 178509801 | HCID 178509801 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 178509799 | HCID 178509799 | 89.3% |
Reaction Steps
A mixture of (2-(1,3-dioxan-2-yl)ethyl)triphenylphosphonium bromide (25.0 g, 54.7 millimols) with THF (150 ml) was cooled down to -20° C., followed by adding t-BuOK (6.1 g, 54.7 millimols) to the mixture, stirring for 30 minutes, dropwise adding to the mixture, a THF (80 ml) solution of trans-4-(trans-4-(4-cyanophenyl)cyclohexyl)cyclohexanecarbaldehyde (14.4 g, 49.8 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 used for extraction was made 400 ml, to obtain raw 4-(trans-4-(trans-4-(3-(1,3-dioxan-2-yl)propenyl)cyclohexyl)cyclohexyl)benzonitrile (17.5 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-a1349c1cfa6d421c9be6f9bfbae78a1e |
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| Source note | uspto-grants-1998_02 |
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