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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 225948Erstellt: 26. Oktober 2026

Phenol → Phenoxymethyl ketone

https://huagongshe.com/reaction/225948

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktPhenolHCID 996—
Edukt1,3-Dibromo-2-propanoneHCID 69952—
EduktPotassium FluorideHCID 522689—
LösungsmittelDimethylformamideHCID 6228—
ProduktPhenoxymethyl ketoneHCID 1340809050%

Reaktionsschritte

Thus obtained bromomethyl ketone derivative (X, 12.9 g, 31.0 mmol) and phenol (3.23 g, 1.2 Eq) were dissolved in dimethylformamide (30 ml), KF(4.53 g, 2.5 Eq) was added, and the mixture was stirred for two hours to give phenoxymethyl ketone derivative (XIb). This compound was dissolved in methanol (40 ml)-THF (100 ml) and was reacted by adding NaBH4 (2.35 g)-methanol solution (40 ml) (−10□-room temperature, two hours). The reaction was stopped by acetic acid, and the reaction mixture was distilled under reduced pressure to remove methanol. The residue was extracted with ethyl acetate (50 ml×2), washed with water and aqueous sodium chloride solution, dried (anhydrous Na2SO4), concentrated under reduced pressure, and separated-purified by column chromatography (ethyl acetate-hexane, 1:7) to give a compound (XIIb, 6.50 g, Yield 50%) in a diastereomeric form of which amino group is protected by benzyloxycarbonyl.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07557133B2
Quelldatensatzuspto-grants-2009_07
ORD IDord-8187fab915144f549df77aa45aa50258
Quellennotizuspto-grants-2009_07