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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1023326Erstellt: 23. Oktober 2026

Iodine → 1-[4-({[Tert-butyl(dimethyl)silyl]oxy}methyl)phenyl]propan-2-ol

https://huagongshe.com/de/reaction/1023326

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktIodineHCID 807—
EduktPropylene OxideHCID 6378—
EduktAmmonium ChlorideHCID 25517—
Edukt4-Bromobenzyloxy-tert-butyldimethylsilaneHCID 10859583—
LösungsmittelTetrahydrofuranHCID 8028—
Produkt1-[4-({[Tert-butyl(dimethyl)silyl]oxy}methyl)phenyl]propan-2-olHCID 67377030—

Reaktionsbedingungen

Temperatur50 °C

Reaktionsschritte

To a solution of (4-bromobenzyloxy)(tert-butyl)dimethylsilane (3.080 g) in THF (20 mL) were added Mg (0.288 g) and I2 (cat) at room temperature under an Ar atmosphere. The mixture was heated at 50° C. for 1 hour, and then cooled to room temperature. To the mixture was added 1,2-epoxypropane (0.77 mL) at room temperature under an Ar atmosphere, and the mixture was stirred at room temperature for 14.5 hours, and then heated at 50° C. for 1 hour, and then cooled to room temperature. To the mixture was added saturated aqueous NH4Cl, and the mixture was extracted with AcOEt. The organic layer was washed with saturated aqueous NaCl, dried over anhydrous Na2SO4, and concentrated under reduced pressure. The residue was purified by silica gel column chromatography (n-hexane/AcOEt=2/1) to afford 1-[4-({[tert-butyl(dimethyl)silyl]oxy}methyl)phenyl]propan-2-ol (1.485 g) as a colorless oil.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08722663B2
Quelldatensatzuspto-grants-2014_05
ORD IDord-3bbe2a901c9b43e794b12ea9324b81fc
Quellennotizuspto-grants-2014_05