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
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Methyl iodide | HCID 6328 | — |
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | 5-Nitro-2,3-dihydro-1,3-benzoxazol-2-one | HCID 263965 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | 2(3H)-benzoxazolone, 3-methyl-5-nitro- | HCID 641557 | — |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US08268820B2 |
|---|
| Source dataset | uspto-grants-2012_09 |
|---|
| ORD ID | ord-78fc961df5ff4971b66cf61d053b455c |
|---|
| Source note | uspto-grants-2012_09 |
|---|