HuagongsheHuagongshe Chemistry Print Report · For research reference only
Methyl acetoacetate → 3-Isopropenyl-4-nitro-2(3H)-benzimidazolone
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Methyl acetoacetate | HCID 7757 | — |
| Reactant | Potassium Hydroxide | HCID 14797 | — |
| Reactant | 3-Nitro-1,2-phenylenediamine | HCID 4359525 | — |
| Reactant | Methanol--water (1/1) | HCID 22242641 | — |
| Solvent | O-Xylene | HCID 7237 | — |
| Product | 3-Isopropenyl-4-nitro-2(3H)-benzimidazolone | HCID 10536836 | — |
Reaction Steps
0.3 ml of 47% potassium hydroxide and then 115 mmol of methyl acetoacetate are added to 100 mmol of 2-amino-3-nitroaniline in 50 ml of xylene brought to 120° C. The whole mixture is brought to reflux for 4 hours and the water/methanol mixture formed is removed by means of a Dean and Stark apparatus. 18 ml of 47% potassium hydroxide and 200 ml of water are then added. The aqueous phase is washed with xylene, brought to pH=6 with 12N hydrochloric acid and then extracted with ethyl acetate and the expected product is purified by chromatography on a silica column, using a dichloromethane/methanol (95/5) mixture as eluent.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05652246 |
| Source dataset | uspto-grants-1997_07 |
| ORD ID | ord-f50582cc8b924b648e0fe750673e8523 |
| Source note | uspto-grants-1997_07 |