HuagongsheHuagongshe Chemistry Print Report · For research reference only
(3-Fluoropropyl)triphenylphosphonium bromide → HCID 178509748, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | (3-Fluoropropyl)triphenylphosphonium bromide | HCID 11429580 | — |
| Reactant | Potassium tert-butoxide | HCID 23665647 | — |
| Reactant | HCID 178509751 | HCID 178509751 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 178509748 | HCID 178509748 | — |
Reaction Conditions
| Temperature | -20 °C |
|---|
Reaction Steps
A mixture of (3-fluoropropyl)triphenylphosphonium bromide (14.7 g, 36.5 millimols) with THF (60 ml) was cooled down to -20° C., followed by adding t-BuOK (4.1 g, 36.5 millimols) to the mixture, stirring for one hour, dropwise adding to the mixture, a THF (50 ml) solution of trans-4-(2-(4-cyanophenyl)ethyl)cyclohexanecarbaldehyde (9.0 g, 30.2 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 product in the same manner as in Example 1 except that the quantity used for extraction was made 200 ml, to obtain raw 4-(2-(trans-4-(4-fluorobutenyl)cyclohexyl)ethyl)benzonitrile (8.1 g).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05653911 |
| Source dataset | uspto-grants-1997_08 |
| ORD ID | ord-24ad9cbf526b477ead54edfb4172a8c7 |
| Source note | uspto-grants-1997_08 |