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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 346584Erstellt: 25. Oktober 2026

Benzyl Bromide → 1-Benzyl-6-methyl-1H-benzo[d][1,3]oxazine-2,4-dione

https://huagongshe.com/reaction/346584

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktBenzyl BromideHCID 7498—
EduktSodium hydrideHCID 24758—
Edukt5-Methylisatoic anhydrideHCID 294478—
LösungsmittelDimethylformamideHCID 6228—
Produkt1-Benzyl-6-methyl-1H-benzo[d][1,3]oxazine-2,4-dioneHCID 2108191697%

Reaktionsschritte

A solution of Compound 11 (25 g, 141 mmol) in DMF was added slowly to a suspension of NaH (60% in mineral oil, 6.21 g, 155 mmol) in DMF and further stirred at room temperature for 1 h. Then, neat benzyl bromide (19.53 mL, 155 mmol) was added and the solution further stirred at room temperature for 3 h. The solution was poured into ice water, and the solids formed were filtered, washed several times by water, and dried. The solid was suspended in hexane, sonicated briefly, filtered, and washed by hexane to yield 36.5 g (97%) of white solids. M.P. 150° C. 1H NMR (DMSO-d6): δ 2.32 (s, 3H), 5.27 (s, 2H), 7.15 (d, J=8.7 Hz, 1H), 7.26–7.39 (m, 5H), 7.54 (dd, J=1.5, 8.7 Hz, 1H), 7.83 (d, J=1.5 Hz, 1H). Anal. (C16H13NO3) C, H, N.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07173036B2
Quelldatensatzuspto-grants-2007_02
ORD IDord-5ce467f7e5fb4262b869e83c7b4868b7
Quellennotizuspto-grants-2007_02