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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 417916Erstellt: 26. Oktober 2026

Chloroacetyl chloride → 6-Bromo-2H-1,4-benzoxazin-3(4H)-one

https://huagongshe.com/reaction/417916

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktChloroacetyl chlorideHCID 6577—
EduktTriethylamineHCID 8471—
EduktSodium hydrideHCID 24758—
Edukt2-Amino-4-BromophenolHCID 351840—
LösungsmittelTetrahydrofuranHCID 8028—
Produkt6-Bromo-2H-1,4-benzoxazin-3(4H)-oneHCID 1621814272,2%

Reaktionsschritte

Triethylamine (2.4 mL, 17 mmol) was added to 2-amino-4-bromophenol (2.5 g, 13 mmol) in THF (80 mL). The reaction was cooled in ice and chloroacetyl chloride (1.12 mL, 14 mmol) added portionwise. It was stirred with cooling for 10 min then allowed to warm to r.t. and stirred for a further 2 h. The reaction mixture was cooled in ice and sodium hydride (1.05 g of a 60% suspension in oil, 26 mmol) was added portionwise. The mixture was stirred with ice-bath cooling for 20 min then at r.t. for 2 h before being quenched with water (20 mL). The THF was removed in vacuo and the resulting mixture diluted with water (100 mL). The precipitate was filtered off, washed with water (3×50 mL) and dried in vacuo to yield the title compound as a beige solid (2.14 g, 70%). δH (DMSO-d6) 4.60 (2H, s), 6.92 (1H, d, J 8.5 Hz), 7.02 (1H, d, J 2.3 Hz), 7.08 (1H, dd, J 8.5, 2.3 Hz), 10.81 (1H, br s).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08093238B2
Quelldatensatzuspto-grants-2012_01
ORD IDord-181b1dc58ad645a9803fe02194e08224
Quellennotizuspto-grants-2012_01