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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1258836Erstellt: 25. Oktober 2026

Triethylsilane → 4-benzyl-6-[(5-bromo-2-chloro-phenyl)methyl]spiro[3H-1,4-benzoxazine-2,1'-cyclopropane]

https://huagongshe.com/reaction/1258836

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktTriethylsilaneHCID 12052—
EduktTrifluoromethanesulfonic acidHCID 62406—
Edukt(4-benzylspiro[3H-1,4-benzoxazine-2,1-cyclopropane]-6-yl)-(5-bromo-2-chloro-phenyl)methanolHCID 58340780—
LösungsmittelTrifluoroacetic acidHCID 6422—
Produkt4-benzyl-6-[(5-bromo-2-chloro-phenyl)methyl]spiro[3H-1,4-benzoxazine-2,1'-cyclopropane]HCID 5834083392,5%

Reaktionsbedingungen

Temperatur50 °C

Reaktionsschritte

To an ice cold solution of (4-benzylspiro[3H-1,4-benzoxazine-2,1-cyclopropane]-6-yl)-(5-bromo-2-chloro-phenyl)methanol (780 mg, 1.7 mmol) in trifluoroacetic acid (4 mL) was added triethylsilane (1.32 mL, 8.3 mmol) followed by triflic acid (0.15 mL, 1.7 mmol). After heating the mixture for 15 min at 50° C., the reaction was cooled to room temperature. Trifluoroacetic acid was evaporated under reduced pressure, and the resulting residue was taken in saturated aq. sodium bicarbonate solution and extracted with ethyl acetate. The organic layer was washed with water, brine, dried over sodium sulfate, and concentrated. The resulting residue was purified by silica gel column chromatography to furnish 4-benzyl-6-[(5-bromo-2-chloro-phenyl)methyl]spiro[3H-1,4-benzoxazine-2,1-cyclopropane] (715 mg).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08466114B2
Quelldatensatzuspto-grants-2013_06
ORD IDord-9a5d4fa348524a2ba827c92400fa11d3
Quellennotizuspto-grants-2013_06