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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2358890Generated: November 1, 2026

Chloride → HCID 86660292, compound

https://huagongshe.com/reaction/2358890

Reaction equation

Participants

RoleNameHCIDCharge
ReactantChlorideHCID 312—
ReactantPotassium tert-butoxideHCID 23665647—
ReactantHCID 67992146HCID 67992146—
SolventTetrahydrofuranHCID 8028—
ProductHCID 86660292HCID 8666029276.2%

Reaction Conditions

Temperature-20 °C

Reaction Steps

Methoxymethyltriphenylphophnium chloride (55.23 g) and THF (300 ml) were placed in a reaction vessel, and the solution was cooled to −20° C. Potassium t-butoxide (16.0 g) was added, and the stirring was continued for another 1 hour. Then, 4-(5-propyltetrahydro-2-furanyl)cyclohexanone (15 g) in a THF (100 ml) solution was added dropwise, and the stirring was continued for another 1 hour. The reaction mixture was warmed to room temperature, and the mixture was separated after the addition of water (200 ml). The organic layer was dried over anhydrous magnesium sulfate and the solvent was distilled off under reduced pressure. The residue was purified by silica gel chromatography (toluene:ethyl acetate=18:1), and the resultant product was dissolved in acetone (200 ml) and hydrochloric acid (6 M) (200 ml) was added, and then the stirring was continued at room temperature for another 1 hour. The mixture was extracted with toluene (100 ml) after the addition of water (200 ml). The solution was dried over anhydrous magnesium sulfate and the solvent was distilled off under reduced pressure to give 4-(5-propyltetrahydro-2-furanyl)cyclohexanecarboaldehyde (12.2 g)

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08685274B2
Source datasetuspto-grants-2014_04
ORD IDord-432dba29ca434bd29faa5f5be639d2a4
Source noteuspto-grants-2014_04