Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 726449Generated: October 30, 2026

Water → HCID 178455764, compound

https://huagongshe.com/reaction/726449

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantMethyltriphenylphosphonium iodideHCID 638159—
ReactantPotassium tert-butoxideHCID 23665647—
ReactantHCID 178501096HCID 178501096—
SolventTetrahydrofuranHCID 8028—
ProductHCID 178455764HCID 17845576449.8%

Reaction Conditions

Temperature-50 °C

Reaction Steps

A mixture of 30.2 g (74.7 mmol) of methyltriphenylphosphonium iodide and 400 ml of THF was cooled to -50° C. To this mixture was added 9.23 g (82.2 mmol) of t-BuOK and the resulting mixture was stirred for one hour. To this mixture was added dropwise a solution of 20.0 g (59.8 mmol) of trans-4-(trans-4-(trans-4-formylcyclohexyl)cyclohexyl)cyclohexane carboxylic acid methyl ester in 500 ml of THF, while maintaining a temperature at below -50° C. After the dropwise addition, the reaction temperature was gradually allowed to rise up to room temperature. After 300 ml of water was added to the reaction mixture, the reaction mixture was extracted with 1000 ml of toluene. The organic layer was washed three times with water and dried over anhydrous magnesium sulfate. The solvent was distilled off under reduced pressure and the residue was subjected to a silica gel column chromatography (a developing solvent: heptane) to give 9.90 g of crude trans-4-(trans-4-(trans-4-ethenylcyclohexyl)cyclohexyl)-cyclohexane carboxylic acid methyl ester.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05709820
Source datasetuspto-grants-1998_01
ORD IDord-cf5e2a0db7d1490887fed64f877322f2
Source noteuspto-grants-1998_01