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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1696695Erstellt: 26. Oktober 2026

Dichloromethane → 2-[(2-Hydroxy-1-methyl-2-{4-[(triisopropylsilyl)oxy]phenyl}ethyl)thio]phenol

https://huagongshe.com/reaction/1696695

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktDichloromethaneHCID 6344—
EduktAmmonium ChlorideHCID 25517—
EduktSodium borohydrideHCID 4311764—
Edukt2-[(2-Hydroxyphenyl)thio]-1-{4-[(triisopropylsilyl)oxy]phenyl}propan-1-oneHCID 67277409—
LösungsmittelMethanolHCID 887—
Produkt2-[(2-Hydroxy-1-methyl-2-{4-[(triisopropylsilyl)oxy]phenyl}ethyl)thio]phenolHCID 67277626106,1%

Reaktionsschritte

With cooling with ice, sodium borohydride (5.5 g, 134 mmol) was added to a dichloromethane (500 mL)/methanol (500 mL) mixed solution of 2-[(2-hydroxyphenyl)thio]-1-{4-[(triisopropylsilyl)oxy]phenyl}propan-1-one (48 g, 112 mmol) obtained in Reference Example 1-2, and stirred for 2 hours with cooling with ice, then restored to room temperature, and further stirred for 40 minutes. Aqueous saturated ammonium chloride solution was added, and stirred for a while, and then the solvent was almost completely evaporated off under reduced pressure. The residue was diluted with ethyl acetate, and extracted with aqueous saturated ammonium chloride solution. The organic layer was dried with sodium sulfate, and concentrated under reduced pressure to obtain a crude product (51.4 g) of the intended compound.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08163770B2
Quelldatensatzuspto-grants-2012_04
ORD IDord-31c3d690cf844e988d754e0954d94b54
Quellennotizuspto-grants-2012_04