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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 726451Generated: October 30, 2026

Water → HCID 178445635, compound

https://huagongshe.com/reaction/726451

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantMethyltriphenylphosphonium iodideHCID 638159—
ReactantPotassium tert-butoxideHCID 23665647—
ReactantHCID 178501095HCID 178501095—
SolventTetrahydrofuranHCID 8028—
ProductHCID 178445635HCID 17844563544.7%

Reaction Conditions

Temperature-50 °C

Reaction Steps

A mixture of 130 g (322 mmol) of methyltriphenylphosphonium iodide and 1.3 liters of THF was cooled to -50° C. To this mixture was added 33.4 g (110 mmol) of t-BuOK and the resulting mixture was stirred for one hour. To this mixture was added dropwise, while maintaining a temperature at below -50° C., a solution of 90.0 g (248 mmol) of crude trans-4-(trans-4-(trans-4-(2-formylethyl)-cyclohexyl)cyclohexyl)cyclohexane carboxylic acid methyl ester in 900 ml of THF. After the dropwise addition, the temperature of the reaction solution was gradually allowed to rise up to room temperature and the mixture was stirred for further 5 hours. After the reaction was completed by adding 500 ml of water, the reaction mixture was filtered through Celite, the solvent was distilled off under reduced pressure and the filtrate was extracted with 1.0 liter of toluene. The organic layer was washed three times with 500 ml of 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: toluene) to give 40.0 g of crude trans-4-(trans-4-(trans-4-(3-butenyl)cyclohexyl)cyclohexyl)-cyclohexane carboxylic acid methyl ester.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05709820
Source datasetuspto-grants-1998_01
ORD IDord-9ca8d8a3cd0e43e89f3fc3b1707de769
Source noteuspto-grants-1998_01