Zurück
HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 66402Erstellt: 24. Oktober 2026

Iodine → 1-Iodo-4-trimethylsiloxy-trans-1-octene

https://huagongshe.com/de/reaction/66402

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktIodineHCID 807—
EduktTrimethylamine oxideHCID 1145—
EduktSodium HydroxideHCID 14798—
EduktBis(1,2-dimethylpropyl)boraneHCID 192733—
EduktTrimethyl[(oct-1-yn-4-yl)oxy]silaneHCID 12786181—
LösungsmittelTetrahydrofuranHCID 8028—
Produkt1-Iodo-4-trimethylsiloxy-trans-1-octeneHCID 12851277—

Reaktionsschritte

To a stirred solution of 0.020 moles of freshly prepared bis-(3-methyl-2-butyl)borane in 300 ml of tetrahydrofuran at 0°-5° C is added dropwise a solution of 19.8 g of 4-trimethylsiloxy-1-octyne in 30 ml of tetrahydrofuran. The resulting mixture is stirred at ambient temperature for several hours, cooled in an ice bath, and treated with 53 g of trimethylamine oxide. The mixture is stirred several hours at 25°-40° C and then poured into 2 liters of 15% sodium hydroxide. The resulting mixture is treated immediately with a solution of 140 g of iodine in 300 ml of tetrahydrofuran. After 0.5 hour the organic phase is separated and the aqueous phase is extracted with ether. The combined organic layers are washed with water, sodium thiosulfate solution, and brine; dried over magnesium sulfate; and concentrated to give an oil, pmr spectrum (CDCl 3): 6.2 (d, ICH=) and 6.7 (quintuplet, =C-).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS04131737
Quelldatensatzuspto-grants-1978_12
ORD IDord-ee8814a93a8044e3904426eff2a6053d
Quellennotizuspto-grants-1978_12