Chloride → HCID 86660292, compound

Temperature

-20 °C

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)

1. waitthe stirring was continued for another 1 hour
2. temperatureThe reaction mixture was warmed to room temperature
3. customthe mixture was separated
4. additionafter the addition of water (200 ml)
5. dry with materialThe organic layer was dried over anhydrous magnesium sulfate
6. distillationthe solvent was distilled off under reduced pressure
7. customThe residue was purified by silica gel chromatography (toluene:ethyl acetate=18:1)
8. dissolutionthe resultant product was dissolved in acetone (200 ml)
9. additionhydrochloric acid (6 M) (200 ml) was added
10. waitthe stirring was continued at room temperature for another 1 hour
11. extractionThe mixture was extracted with toluene (100 ml)
12. additionafter the addition of water (200 ml)
13. dry with materialThe solution was dried over anhydrous magnesium sulfate
14. distillationthe solvent was distilled off under reduced pressure

ORD record

ord-432dba29ca434bd29faa5f5be639d2a4

Source dataset

uspto-grants-2014_04

DOI

10.6084/m9.figshare.5104873.v1

Patent number

US08685274B2