Back
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

Reaction equation

Participants

RoleNameHCIDCharge
Reactant(3-Fluoropropyl)triphenylphosphonium bromideHCID 11429580—
ReactantPotassium tert-butoxideHCID 23665647—
ReactantHCID 178444507HCID 178444507—
SolventTetrahydrofuranHCID 8028—
ProductHCID 178444499HCID 17844449987.8%

Reaction Conditions

Temperature-20 °C

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05720899
Source datasetuspto-grants-1998_02
ORD IDord-153282506a144b27a4782ff732c7f6f3
Source noteuspto-grants-1998_02