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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1696300Erstellt: 27. Oktober 2026

Acetyl chloride → ethyl 4-acetyl-3,4-dihydro-2H-1,4-benzoxazine-2-carboxylate

https://huagongshe.com/reaction/1696300

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktAcetyl chlorideHCID 6367—
EduktEthyl 3,4-dihydro-2H-1,4-benzoxazine-2-carboxylateHCID 31090—
EduktDiisopropylethylamineHCID 81531—
Katalysator4-(Dimethylamino)pyridineHCID 14284—
LösungsmittelDichloromethaneHCID 6344—
Produktethyl 4-acetyl-3,4-dihydro-2H-1,4-benzoxazine-2-carboxylateHCID 1342508366,7%

Reaktionsbedingungen

Temperatur25 °C

Reaktionsschritte

Acetyl chloride (23 L, 0.33 mmol) was added to a solution of (±)-ethyl 3,4-dihydro-2H-benzo[b][1,4]oxazine-2-carboxylate (Example 3a, 55 mg, 0.27 mmol), DMAP (1.6 mg, 0.013 mmol), and Hunig's base (63 L, 0.36 mmol) in dichloromethane (2 mL). The solution was stirred at 25° C. for 24 h, then the reaction mixture was diluted with dichloromethane (60 mL) and the mixture was extracted with 0.1 M sodium carbonate (7 mL) and half-saturated brine (7 mL). The organic layer was dried over sodium sulfate and concentrated. Purification of the product by flash column chromatography (40% EtOAc/hexane) afforded the title compound (46 mg, 0.18 mmol). MS m/z: 250 (M+1).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08163766B2
Quelldatensatzuspto-grants-2012_04
ORD IDord-d9b93c1dee6f47228a481e2b53d3e33d
Quellennotizuspto-grants-2012_04