Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1991336Generated: October 27, 2026

Methyl iodide → 4-fluoro-3-methyl-6-nitro-1,3-benzoxazol-2(3H)-one

https://huagongshe.com/reaction/1991336

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethyl iodideHCID 6328—
Reactant1,8-Diazabicyclo(5.4.0)undec-7-eneHCID 81184—
Reactant4-fluoro-6-nitro-1,3-benzoxazol-2(3H)-oneHCID 68489292—
SolventDimethylformamideHCID 6228—
SolventEthyl AcetateHCID 8857—
Product4-fluoro-3-methyl-6-nitro-1,3-benzoxazol-2(3H)-oneHCID 6848715283.1%

Reaction Conditions

Temperature65 °C

Reaction Steps

Iodomethane (0.393 ml, 6.31 mmol) is added in portions to crude 4-fluoro-6-nitro-1,3-benzoxazol-2(3H)-one (Step 5, 1.00 g, 5.05 mmol) and 1,8-diazabicyclo[5.4.0]undec-7-ene (0.94 ml, 6.31 mmol) in DMF (10 ml). The reaction is stirred at 65° C. overnight, diluted with ethyl acetate, washed with 2N HCl and saline, dried (MgSO4), and evaporated to give crude product containing trace amounts of undesired 5-nitro isomer. Purification by flash column chromatography (20% ethyl acetate/hexane) gives pure product as a white solid (0.89 g, 83%); mp 118-9° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07645781B2
Source datasetuspto-grants-2010_01
ORD IDord-8282183087ff4b039ed88e9d7cefc12b
Source noteuspto-grants-2010_01