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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1172992Erstellt: 25. Oktober 2026

Sodium Hydroxide → 3-Methyl-3,4-dihydro-2H-1,4-benzoxazine

https://huagongshe.com/reaction/1172992

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktSodium HydroxideHCID 14798—
Edukt2H-1,4-benzoxazin-3(4H)-oneHCID 72757—
EduktSodium borohydrideHCID 4311764—
EduktHCID 178418332HCID 178418332—
LösungsmittelTetrahydrofuranHCID 8028—
LösungsmittelEthyl AcetateHCID 8857—
Produkt3-Methyl-3,4-dihydro-2H-1,4-benzoxazineHCID 276376046%

Reaktionsbedingungen

Temperatur50 °C

Reaktionsschritte

To a solution of 2H-1,4-benzoxazin-3(4H)-one (2.00 g, 13.4 mmol) in tetrahydrofuran (20 ml) was added dropwise at 5° C. a THF solution of methylmagnesium chloride (17.9 ml, 3 M, 53.7 mmol) and the reaction mixture was then stirred at 50° C. for 90 min. The reaction mixture was then cooled to 5° C. and quenched by dropwise addition of 20 ml acetic acid. Sodium borohydride (1.27 g, 33.5 mmol) was then added portionwise and the mixture was stirred at room temperature overnight. The resulting suspension was then cooled to 0° C. and 3 N aq. sodium hydroxide solution was added dropwise until the mixture was pH 10. Ethyl acetate was then added, the phases separated, and the organic phase dried over sodium sulphate and concentrated in vacuo. The residue was purified by chromatography on silica gel (eluant: heptane/ethyl acetate gradient) to yield the title compound as a colorless oil (0.92 g, 46%); MS (ISP): 150.3 ([M+H]+).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07834044B2
Quelldatensatzuspto-grants-2010_11
ORD IDord-4f5fa2ca77274077b24abc3683f37896
Quellennotizuspto-grants-2010_11