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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1435803Erstellt: 25. Oktober 2026

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

https://huagongshe.com/reaction/1435803

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%): mp: 199-201° C.; 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
PatentnummerUS07618958B2
Quelldatensatzuspto-grants-2009_11
ORD IDord-4600d3862d0b4b4caf676671d40f5734
Quellennotizuspto-grants-2009_11