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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 970475Generated: October 26, 2026

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

https://huagongshe.com/reaction/970475

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzyl BromideHCID 7498—
ReactantSodium hydrideHCID 24758—
Reactant5-Methylisatoic anhydrideHCID 294478—
SolventDimethylformamideHCID 6228—
Product1-Benzyl-6-methyl-1H-benzo[d][1,3]oxazine-2,4-dioneHCID 2108191697%

Reaction Steps

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.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07312220B2
Source datasetuspto-grants-2007_12
ORD IDord-cf41f1b0a3434b63aea7ec75cbf168e8
Source noteuspto-grants-2007_12