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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 38651Erstellt: 24. Oktober 2026

Triethylamine → N-(6-acetyl-1,3-benzodioxol-5-yl)-1-benzofuran-3-carboxamide

https://huagongshe.com/de/reaction/38651

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktTriethylamineHCID 8471—
Edukt1-(6-Amino-1,3-benzodioxol-5-yl)ethan-1-oneHCID 120000—
Edukt1-Benzofuran-3-carbonyl chlorideHCID 13024720—
LösungsmittelTolueneHCID 1140—
ProduktN-(6-acetyl-1,3-benzodioxol-5-yl)-1-benzofuran-3-carboxamideHCID 44220313—

Reaktionsbedingungen

Temperatur20 °C

Reaktionsschritte

Into solutions of 154 (5.0 mmol) in 200 mL of dry toluene were added triethylamine (4 mL) and 2-amino-4,5-methylenedioxy acetophenone (148) (5 mmol). The mixtures were stirred at 20±2° C. for 24 h and then evaporated. The residues were washed with acetone and EtOH and then recrystallized from acetone or EtOH to form 155. Obtained as a pale-yellow solid; mp 144-145° C.; ESI-MS (Positive mode): m/z 324 [M+H]+; 1H-NMR (400 MHz, DMSO-d6): δ 2.63 (3H, s), 6.19 (2H, s), 7.41-7.50 (21-1, m), 7.68 (1H, s), 7.75 (1H, dd, J=1.6, 6.8 Hz), 8.15 (1H, dd, J=2.0, 8.8 Hz), 8.27 (1H, s), 8.71 (1H, s), 12.63 (1H, s); IR (KBr): 1635, 1677 (C═O) cm−1.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08524740B2
Quelldatensatzuspto-grants-2013_09
ORD IDord-f9b04acd88cd445f8767056ebf37512a
Quellennotizuspto-grants-2013_09