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HRID 229943Erstellt: 24. Oktober 2026

Citric Acid → Methyl (5Z)-(9R,11R,13RS,14RS,15S)-9-chloro-11,15-dihydroxy-16,16-dimethyl-13,14-epoxy-5-prostenoate

https://huagongshe.com/de/reaction/229943

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktCitric AcidHCID 311—
Edukttert-Butyl hydroperoxideHCID 6410—
EduktMethyl (5Z,13E,15R)-9beta-chloro-11alpha,15-dihydroxy-16,16-dimethylprosta-5,13-dien-1-oateHCID 13853250—
KatalysatorTitanium isopropoxideHCID 11026—
KatalysatorFerrous SulfateHCID 24393—
LösungsmittelWaterHCID 962—
LösungsmittelDichloromethaneHCID 6344—
ProduktMethyl (5Z)-(9R,11R,13RS,14RS,15S)-9-chloro-11,15-dihydroxy-16,16-dimethyl-13,14-epoxy-5-prostenoateHCID 57759195—

Reaktionsbedingungen

Temperatur-20 °C

Reaktionsschritte

4.7 mL of titanium(IV) isopropoxide are added dropwise to a solution of 6.52 g of methyl (5Z,13E)-(9R,11R,15R)-9-chloro-11,15-dihydroxy-16,16-dimethyl-5,13-prostadienoate in 33 mL of methylene chloride at −20° C. under nitrogen, and the mixture is stirred at −20° C. for 30 min. Six mL of tert-butyl hydroperoxide are then added to the reaction mixture. A solution of 10 g of iron sulphate and 20 g of citric acid in 100 mL of water is subsequently added, and the mixture is extracted 3× with methylene chloride. The combined organic phases are washed 1× with saturated sodium chloride solution, dried over sodium sulphate and concentrated in vacuo. Chromatography on silica gel with methylene chloride/ethyl acetate (0-40%) results in 3.55 g of the epoxide as a colourless oil.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07563924B2
Quelldatensatzuspto-grants-2009_07
ORD IDord-585aaab029684af5995ae20f693cc2a5
Quellennotizuspto-grants-2009_07