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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1487200Erstellt: 26. Oktober 2026

Acetic Anhydride → N-(2,3-dihydro-1,4-benzodioxin-5-yl)acetamide

https://huagongshe.com/reaction/1487200

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktAcetic AnhydrideHCID 7918—
Edukt2,3-Dihydro-1,4-benzodioxin-5-amineHCID 11788387—
LösungsmittelEthanolHCID 702—
ProduktN-(2,3-dihydro-1,4-benzodioxin-5-yl)acetamideHCID 65859395%

Reaktionsschritte

To a solution of 2,3-dihydrobenzo[b][1,4]dioxin-5-amine (Intermediate B3, 4.5 g, 30 mmol) in ethanol (50 mL) at room temperature was slowly added acetic anhydride (3.0 g, 30 mmol). After the addition was over, the mixture was stirred at room temperature for 5 minutes. The resulting suspension was concentrated to give the crude product, which was purified by silica gel column chromatography (petroleum ether/ethyl acetate 4/1) to afford the product N-(2,3-dihydrobenzo[b][1,4]dioxin-5-yl)acetamide (5.5 g, yield 95%). 1H NMR (400 MHz, CDCl3) δ ppm 9.12 (s, 1H), 7.44-7.46 (d, 1H, J=8.0 Hz), 6.71-6.75 (t, 1H, J=8.0 Hz), 6.59-6.61 (d, 1H, J=7.6 Hz), 4.23-4.30 (m, 4H), 2.06 (s, 3H).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS09428508B2
Quelldatensatzuspto-grants-2016_08
ORD IDord-aad21df284a645318e6f503c791ea2df
Quellennotizuspto-grants-2016_08