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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 249165Erstellt: 25. Oktober 2026

Phenothiazine → Tert-butyl 3-(phenothiazin-10-ylmethyl)benzoate

https://huagongshe.com/reaction/249165

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktPhenothiazineHCID 7108—
EduktMethyl 3-(chloromethyl)benzoateHCID 3248988—
EduktPotassium tert-butoxideHCID 23665647—
LösungsmittelTetrahydrofuranHCID 8028—
ProduktTert-butyl 3-(phenothiazin-10-ylmethyl)benzoateHCID 1902481030,6%

Reaktionsbedingungen

Temperatur0 °C

Reaktionsschritte

To a solution of phenothiazine (1.00 g) in tetrahydrofuran (10 ml) was added potassium tert-butoxide (617 mg) at 0° C. The mixture was stirred at 0° C. for 20 minutes, and then a solution of methyl 3-(chloromethyl)benzoate (1.02 g) in tetrahydrofuran (10 ml) was added. The mixture was stirred at 25° C. for 3 hours, and then potassium tert-butoxide (1.02 g) was added. The mixture was stirred at 25° C. for 1 hour, 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 chromatographed on silica gel eluting with a mixture of hexane and ethyl acetate (40:1) to give tert-butyl 3-(phenothiazin-10-ylmethyl)benzoate (598 mg) as crystals.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS05212320
Quelldatensatzuspto-grants-1993_05
ORD IDord-5de86612323143d4aaac4815ed542123
Quellennotizuspto-grants-1993_05