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HRID 1091748Erstellt: 26. Oktober 2026

4,5-Dichlorophthalic anhydride → (Z)-5,6-dichloro-3-(4-fluoro-3-(4-methoxypiperidine-1-carbonyl)benzylidene)isobenzofuran-1(3H)-one

https://huagongshe.com/reaction/1091748

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
Edukt4,5-Dichlorophthalic anhydrideHCID 70334—
EduktSodium AcetateHCID 517045—
EduktAluminumHCID 5359268—
Edukt2-(4-fluoro-3-(4-methoxypiperidine-1-carbonyl)phenyl)acetic AcidHCID 57791763—
Produkt(Z)-5,6-dichloro-3-(4-fluoro-3-(4-methoxypiperidine-1-carbonyl)benzylidene)isobenzofuran-1(3H)-oneHCID 5779185316,92%

Reaktionsbedingungen

Temperatur240 °C

Reaktionsschritte

A flask charged with 5,6-dichloroisobenzofuran-1,3-dione (370 mg, 1.71 mmol), 2-(4-fluoro-3-(4-methoxypiperidine-1-carbonyl)phenyl)acetic acid (43) (496 mg, 1.68 mmol) and Sodium acetate (34 mg, 0.41 mmol) was lowered into a pre-heated aluminium block at 210° C. The resulting mixture was heated further and stirred at 240° C. for 1 hour then cooled. The residue was triturated, with sonication, under ethanol (˜25 mL) and solid collected by suction filtration to afford crude product (128 mg, 16.92%), which was used directly without further purification; m/z (LC-MS, ESI+), RT=2.79 (M+H 450.1 & 452.0).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08129380B2
Quelldatensatzuspto-grants-2012_03
ORD IDord-38e45d7b8a4040939d9ac32bbf0713f4
Quellennotizuspto-grants-2012_03