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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1768330Erstellt: 25. Oktober 2026

Benzoyl chloride → 6-bromo-2-phenyl-4H-benzo[d][1,3]oxazin-4-one

https://huagongshe.com/reaction/1768330

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktBenzoyl chlorideHCID 7412—
Edukt2-Amino-5-bromobenzoic acidHCID 79858—
Produkt6-bromo-2-phenyl-4H-benzo[d][1,3]oxazin-4-oneHCID 35041197,4%

Reaktionsschritte

The 2-amino-5-bromobenzoic acid (5 g, 23.1 mmol) was treated with benzoyl chloride (237 mL, 2.04 mol) at 140° C. for 3 h. After the reaction mixture was cooled to rt, the crystals that formed were collected by filtration and were washed with hexanes to provide 64 as light brown needles (6.8 g, 97%): 1H NMR (CDCl3) δ 7.51-7.2 (m, 4H), 7.9 (dd, 1H, J=2.3, 8.6 Hz), 8.30-8.33 (m, 2H), 8.8 (d, 1H, J=2.2 Hz); 13C NMR (CDCl3) δ 158.19, 157.35, 145.75, 139.58, 132.82, 130.97, 129.77, 128.82, 128.73, 128.29, 121.37, 118.27; MS (EI) m/e (relative intensity) 303 (M+, 36), 301 (M+, 36), 259 (14), 257 (14), 226 (6), 224 (6), 178 (9), 170 (9), 168 (9), 151 (4), 105 (100).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07235656B2
Quelldatensatzuspto-grants-2007_06
ORD IDord-a48c0e95461c40989205d670c90e0dd3
Quellennotizuspto-grants-2007_06