Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 346608Generated: October 27, 2026

Methyl iodide → 6-Fluoro-1-methyl-2H-3,1-benzoxazine-2,4(1H)-dione

https://huagongshe.com/reaction/346608

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethyl iodideHCID 6328—
ReactantSodium hydrideHCID 24758—
Reactant5-Fluoroisatoic anhydrideHCID 288560—
SolventDimethylformamideHCID 6228—
Product6-Fluoro-1-methyl-2H-3,1-benzoxazine-2,4(1H)-dioneHCID 1271323057%

Reaction Steps

A solution of Compound 35 (3 g, 16.57 mmol) in DMF was added slowly to a suspension of NaH (60% in mineral oil, 0.729 g, 18.23 mmol) in DMF and further stirred at room temperature for 1 h. Then, neat methyl iodide (1.14 mL, 18.23 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 solids were suspended in hexane, sonicated briefly, filtered, and washed by hexane to yield 1.84 g (57%) of white solids. M.P. 133° C. 1H NMR (DMSO-d6): δ3.90 (s, 3H), 7.51 (dd, J=4.0, 8.8 Hz, 1H), 7.77 (m, 12). Anal. (C9H6FNO3) C, H, N.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07173036B2
Source datasetuspto-grants-2007_02
ORD IDord-74ef3fd4f2ea4b88a34126a27348bcb7
Source noteuspto-grants-2007_02