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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 249164Erstellt: 24. Oktober 2026

Phenoxazine → Methyl 3-(phenoxazin-10-ylmethyl)benzoate

https://huagongshe.com/de/reaction/249164

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktPhenoxazineHCID 67278—
EduktMethyl 3-(chloromethyl)benzoateHCID 3248988—
EduktPotassium tert-butoxideHCID 23665647—
LösungsmittelTetrahydrofuranHCID 8028—
ProduktMethyl 3-(phenoxazin-10-ylmethyl)benzoateHCID 1902478928,1%

Reaktionsbedingungen

Temperatur0 °C

Reaktionsschritte

To a solution of phenoxazine (2.20 g) in tetrahydrofuran (30 ml) was added potassium tert-butoxide (2.69 g) at 0° C. The mixture was stirred at 0° C. for 10 minutes, and then a solution of methyl 3-(chloromethyl)benzoate (2.44 g) in tetrahydrofuran (20 ml) was added. The mixture was stirred at 25° C. for 30 minutes, and then evaporated. The residue was partitioned between ethyl acetate and 0.1N hydrochloric acid. The organic layer was washed with water and brine, dried over magnesium sulfate, and evaporated. The residue was purified by chromatography on silica gel eluting with a mixture of hexane and ethyl acetate (40:1-20:1) and recrystallization from a mixture of hexane and ethyl acetate to give e methyl 3-(phenoxazin-10-ylmethyl)benzoate (1.12 g) as crystals.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS05212320
Quelldatensatzuspto-grants-1993_05
ORD IDord-57ce5d9c815f4eb8ba5707df759e45f9
Quellennotizuspto-grants-1993_05