Zurück
HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 257821Erstellt: 25. Oktober 2026

Dichloromethane → 4-Tert-butyldimethylsilyloxymethyl-2-allylphenol

https://huagongshe.com/reaction/257821

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktDichloromethaneHCID 6344—
EduktTriethylamineHCID 8471—
Edukttert-Butyldimethylsilyl chlorideHCID 28928—
Edukt(4-(Prop-2-en-1-yloxy)phenyl)methanolHCID 11744970—
LösungsmittelEthyl AcetateHCID 8857—
Produkt4-Tert-butyldimethylsilyloxymethyl-2-allylphenolHCID 19934838—

Reaktionsschritte

To a solution of the product of Step A (650 mg, 3.96 mmol) in CH2Cl2 (20 mL), cooled to 0° C. under nitrogen, was added triethylamine (612 mL, 4.39 mmol) and a solution of tert-butyldimethylsilyl chloride (631 mg; 4.19 mmol) in CH2Cl2 (2 mL). After stirring at room temperature for 18 hours, the reaction mixture was diluted with ethyl acetate (60 mL), washed with water, and saturated sodium bicarbonate, and then dried (MgSO4). The filtrate was concentrated in vacuo to afford 1.1 g of the title compound which was used crude in the next reaction (Rf =0.45, 5% ethyl acetate/hexanes).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS05264439
Quelldatensatzuspto-grants-1993_11
ORD IDord-5d8d2590ded8469297d4eab6f0d4da32
Quellennotizuspto-grants-1993_11