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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1250128Generated: November 1, 2026

Water → HCID 178447949, compound

https://huagongshe.com/reaction/1250128

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
Reactant4-CyanobenzaldehydeHCID 66042—
ReactantPotassium tert-butoxideHCID 23665647—
ReactantHCID 178448103HCID 178448103—
SolventTetrahydrofuranHCID 8028—
ProductHCID 178447949HCID 17844794947.8%

Reaction Conditions

Temperature-20 °C

Reaction Steps

To a mixture of 25.0 g (0.11 mol) of trans-4-propylcyclohexylmethyltriphenylphosphonium bromide and 100 ml of tetrahydrofuran (THF) was added 12.2 g (0.10 mol) of t-BuOK while maintaining a temperature of lower than −20° C., and stirred for 1 hour. Subsequently, 70 ml of solution of 12.9 g (0.10 mol) of 4-cyanobenzaldehyde in THF was added dropwise to the solution while maintaining a temperature of lower than −20° C., and stirred at the same temperature for 2 hours to react. After finishing of the reaction, 50 ml of water was added to the reaction product and then extracted with 100 ml of toluene. The organic layer thus obtained was washed with water thrice and then dried over anhydrous magnesium sulfate. The solvent was distilled off under a reduced pressure, and the residue was subjected to silica gel column chromatography (eluent: toluene) to obtain 12.1 g of a crude 4-(2-(trans-4-propylcyclohexyl)vinyl)benzonitrile.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06337034B1
Source datasetuspto-grants-2002_01
ORD IDord-7c66edf6096441e882a3cda6a98b29e2
Source noteuspto-grants-2002_01