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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 544868Erstellt: 25. Oktober 2026

4-Ethoxybenzoyl Chloride → 4-ethoxyphenyl 4-fluoro-1-(2,3,4,6-tetra-O-acetyl-beta-D-gluco-pyranosyl)indol-3-yl ketone

https://huagongshe.com/reaction/544868

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
Edukt4-Ethoxybenzoyl ChlorideHCID 140059—
Edukt4-Fluoro-1-(2,3,4,6-tetra-O-acetyl-beta-D-glucopyranosyl)indoleHCID 67020413—
Produkt4-ethoxyphenyl 4-fluoro-1-(2,3,4,6-tetra-O-acetyl-beta-D-gluco-pyranosyl)indol-3-yl ketoneHCID 67196421—

Reaktionsschritte

4-Fluoro-1-(2,3,4,6-tetra-O-acetyl-β-D-glucopyranosyl)-indole obtained in Example 2-(3) and 4-ethoxybenzoyl chloride were treated in a manner similar to Example 2-(4) to give 4-ethoxyphenyl 4-fluoro-1-(2,3,4,6-tetra-O-acetyl-β-D-gluco-pyranosyl)indol-3-yl ketone as a colorless powder. APCI-Mass m/Z 614 (M+H). 1H-NMR (DMSO-d6) δ 1.38 (t, J=6.9 Hz, 3H), 1.68 (s, 3H), 1.97 (s, 3H), 1.98 (s, 3H), 2.04 (s, 3H), 4.11 (d, J=4.0 Hz, 2H), 4.16 (q, J=7.0 Hz, 2H), 4.28-4.31 (m, 1H), 5.30 (t, J=9.8 Hz, 1H), 5.54 (t, J=9.6 Hz, 1H), 5.76 (t, J=9.3 Hz, 1H), 6.34 (d, J=9.0 Hz, 1H), 7.01 (dd, J=10.6, 8.0 Hz, 1H), 7.07 (d, J=8.7 Hz, 2H), 7.36 (td, J=8.1, 4.9 Hz, 1H), 7.62 (d, J=8.3 Hz, 1H), 7.83 (d, J=8.8 Hz, 2H), 8.14 (s, 1H).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07935674B2
Quelldatensatzuspto-grants-2011_05
ORD IDord-96088ff4485742918b7d0be1aae3157d
Quellennotizuspto-grants-2011_05