Diisopropylamine → HCID 53727906, Verbindung

Temperatur

-50 °C

In a 1 flask were charged 370 ml of dried THF and 38.4 g of diisopropylamine in a nitrogen stream, and the solution was cooled to -10° to -5° C. To the solution was added dropwise a 1.6 mole/l hexane solution of 238 ml of n-butyllithium at that temperature over 30 minutes, followed by stirring at that temperature for 1 hour. To the mixture was further added dropwise a solution of 44 g of t-butyl acetate in 44 ml of dried THF over 30 minutes while keeping at that temperature, followed by stirring for 1 hour. The resulting reaction mixture was cooled to -50° C., and a solution of 24 g of methyl (R)-3-methylheptanoate in 24 ml of dried THF was added thereto dropwise over 30 minutes, followed by allowing the mixture to further react at that temperature for 1.5 hours. After the reaction, a saturated ammonium chloride aqueous solution was added to the reaction mixture, and the mixture was extracted with diethyl ether. The extract was washed twice with a sodium chloride aqueous solution, and the solvent was removed by distillation under reduced pressure to obtain 45.2 g of a crude product. Purification by silica gel column chromatography gave 31.0 g (84.0%) of the titled compound.

1. temperaturethe solution was cooled to -10° to -5° C
2. stirringby stirring for 1 hour
3. customThe resulting reaction mixture
4. waitdropwise over 30 minutes
5. customto further react at that temperature for 1.5 hours
6. customAfter the reaction
7. extractionthe mixture was extracted with diethyl ether
8. washThe extract was washed twice with a sodium chloride aqueous solution
9. customthe solvent was removed by distillation under reduced pressure
10. customto obtain 45.2 g of a crude product
11. customPurification by silica gel column chromatography

ORD-Eintrag

ord-4d4219889c5b4b2d868db43452f7dcea

Quelldatensatz

uspto-grants-2000_07

DOI

10.6084/m9.figshare.5104873.v1

Patentnummer

US06093345