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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1112692Erstellt: 25. Oktober 2026

Iodine → 4,4-Dimethyl-1-iodo-trans-1-octen-3-ol

https://huagongshe.com/reaction/1112692

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktIodineHCID 807—
EduktSodium HydroxideHCID 14798—
EduktSodium ThiosulfateHCID 24477—
EduktEthanamine, N,N-diethyl-, N-oxideHCID 123168—
EduktBis(1,2-dimethylpropyl)boraneHCID 192733—
Edukt2-[(4,4-Dimethyloct-1-YN-3-YL)oxy]oxaneHCID 14516370—
LösungsmittelWaterHCID 962—
LösungsmittelTetrahydrofuranHCID 8028—
LösungsmittelDiglymeHCID 8150—
Produkt4,4-Dimethyl-1-iodo-trans-1-octen-3-olHCID 20465723—

Reaktionsschritte

To 233 ml. of a 0.43M solution of disiamylborane in diglyme cooled to 0° C. under an inert atmosphere is added 23.8 g. (0.100 mole) 4,4-dimethyl-3-tetrahydropyranyloxy-1-octyne (Example 995). The mixture is allowed to come to room temperature and is stirred at ambient temperature for 3 hours. The solution is cooled to 0° C. and 22.5 g. (0.30 mole) of triethylamine oxide is added portionwise such that the temperature is maintained at 0°-5° C. The mixture is stirred at 0° C. for 1 hour and is then poured into 150 ml. of 1 N sodium hydroxide followed immediately by a solution of 25.4 g. (0.100 mole) of iodine in 60 ml. of tetrahydrofuran. The mixture is stirred at ambient temperatures for 0.5 hour and poured into 500 ml. of water. The mixture is decolorized by addition of sodium thiosulfate solution and is extracted into ether. The organic phase is washed with water and the solvent is removed in vacuo. The residue is stirred at room temperature for 20 hours with 900 ml. 3:1:1 tetrahydrofuran-acetic acid-water. The solution is evaporated in vacuo and the residue is chromatographed on silica gel in benzene using 10-20% ethylacetate in benzene.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS04123456
Quelldatensatzuspto-grants-1978_10
ORD IDord-95b9780a69bf41c091bc8244895f9e14
Quellennotizuspto-grants-1978_10