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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2386807Generated: October 25, 2026

Methyl iodide → 2(3H)-benzoxazolone, 3-methyl-5-nitro-

https://huagongshe.com/reaction/2386807

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethyl iodideHCID 6328—
ReactantSodium hydrideHCID 24758—
Reactant5-Nitro-2,3-dihydro-1,3-benzoxazol-2-oneHCID 263965—
SolventDimethylformamideHCID 6228—
Product2(3H)-benzoxazolone, 3-methyl-5-nitro-HCID 641557—

Reaction Conditions

Temperature0 °C

Reaction Steps

A solution of 5-nitro-3H-benzooxazol-2-one (26 g) in DMF (100 mL) was added to a suspension of NaH (60% in mineral oil, 10.71 g) in DMF (100 mL) over a period of 1 hour. Stirring was continued for 45 minutes at r.t. The mixture was cooled to 0° C. and methyl iodide dissolved in DMF (20 mL) was added dropwise over a period of 30 minutes. The mixture was stirred over night at r.t. The reaction mixture was poured into ice/water and extracted two times with ethyl acetate. The combined organic layers were washed with brine, dried over Na2SO4, filtered and the solvent was evaporated. CH2Cl2:methanol=4:1 (150 mL) was added to the resulting precipitate and the suspension was stirred for 1 hour at r.t. The solid was filtered off and dried in vacuo. The title compound was obtained as a orange solid (18.33 g, 62%). MS (EI)=194.0 [M+].

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08268820B2
Source datasetuspto-grants-2012_09
ORD IDord-78fc961df5ff4971b66cf61d053b455c
Source noteuspto-grants-2012_09