Hexane → 2-(4-Trifluoromethylphenyl)-3,3,3-trifluoropropenyl methyl ether

Temperatur

-20 °C

Under a nitrogen atmosphere, 25.0 ml of n-butyllithium/hexane solution (1.2M solution) was added to a solution of 12.7 g of methoxymethyltriphenylphosphonium chloride in 100 ml of dry THF at -60° C. The reaction solution was stirred at -60° C. for 30 minutes and at -20° C. for 30 minutes. A solution of 6.0 of 4-trifluoromethyl-α,α,α-trifluoroacetophenone in 10 ml of dry THF was slowly added to the reaction solution at -60° C. The reaction solution was stirred at -60° C. for 1 hour and at room temperature for 14 hours. Thereafter, 150 ml of n-hexane was added to the reaction mixture and insoluble materials were filtered out. The filtrate was washed with dilute HCl-ice water and saturated sodium chloride solution successively and dried over anhydrous magnesium sulfate. The solvent was removed under reduced pressure and 6.1 g of the crude product (E/Z=ca. 1/1) was obtained.

1. stirringThe reaction solution was stirred at -60° C. for 1 hour and at room temperature for 14 hours
2. filtrationwere filtered out
3. washThe filtrate was washed with dilute HCl-ice water and saturated sodium chloride solution successively
4. dry with materialdried over anhydrous magnesium sulfate
5. customThe solvent was removed under reduced pressure

ORD-Eintrag

ord-bf5cfe75cae343d6a4fffce8bf6bfe47

Quelldatensatz

uspto-grants-1989_06

DOI

10.6084/m9.figshare.5104873.v1

Patentnummer

US04840971