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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 567623Generated: October 30, 2026

Methoxymethyl-triphenylphosphonium chloride → HCID 178445634, compound

https://huagongshe.com/reaction/567623

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethoxymethyl-triphenylphosphonium chlorideHCID 2723798—
ReactantPotassium tert-butoxideHCID 23665647—
ReactantHCID 178445639HCID 178445639—
SolventTetrahydrofuranHCID 8028—
ProductHCID 178445634HCID 17844563439.1%

Reaction Conditions

Temperature-50 °C

Reaction Steps

A mixture of 66.4 g (193.7 mmol) of methoxymethyltriphenyl phosphonium chloride and 600 ml of THF was cooled to −50° C. under a gas stream of nitrogen. To the mixture, 20.1 g (179.1 mmol) of t-BuOK was added and stirred for 1 hour. To the mixture, a solution of 37.0 g (148.9 mmol) of trans-4-(trans-4-(3-_butenyl)cyclohexyl)cyclohexane carbaldehyde in 400 ml of THF was added dropwise with maintaining the temperature below −50° C. After dropwise addition, the reaction temperature was increased gradually to the room temperature, and stirring was carried out further for 5 hours. The solvent was distilled off under a decresed pressure, 250 ml of water was added and the mixture was extracted with 300 ml of toluene. The organic layer was washed with 200 ml of water for three times and dried with anhydrous magnesium sulphate. The solvent was distilled off under a decreased pressure, and the residue was subjected to silica gel column chromatography (eluent: a mixed solvent of toluene/heptane=3/7), to obtain 16.1 g of crude 1-(2-methoxyethenyl)-trans-4- (trans-4-(3-butenyl) cyclohexyl) cyclohexane.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06180027B2
Source datasetuspto-grants-2001_01
ORD IDord-a0530a279af54064af044b9d054a6632
Source noteuspto-grants-2001_01