HuagongsheHuagongshe Chemistry Print Report · For research reference only
4-[4-[(E)-C-methyl-N-phenylmethoxycarbonimidoyl]phenyl]-1,2,4-triazolidine-3,5-dione → 4-[4-[(E)-C-methyl-N-phenylmethoxycarbonimidoyl]phenyl]-1,2,4-triazole-3,5-dione
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 4-[4-[(E)-C-methyl-N-phenylmethoxycarbonimidoyl]phenyl]-1,2,4-triazolidine-3,5-dione | HCID 89392333 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 4-[4-[(E)-C-methyl-N-phenylmethoxycarbonimidoyl]phenyl]-1,2,4-triazole-3,5-dione | HCID 89392357 | 52% |
Reaction Steps
To (E)-4-(4-(1-(benzyloxyimino)ethyl)phenyl)-1,2,4-triazolidine-3,5-dione (I-5a: 56 mg, 0.173 mmol) in CH2Cl2 (1.727 mL) was added SiO2—HNO3 (112 mg). The mixture was stirred at room temperature for 30 minutes, filtered, concentrated in vacuo and dried to give (E)-4-(4-(1-(benzyloxyimino)ethyl)phenyl)-3H-1,2,4-triazole-3,5(4H)-dione (I-4b: 29 mg, 52%) as a red solid. 1H NMR (400 MHz, CD3CN) δ ppm 2.31 (s, 3 H) 5.28 (s, 2 H) 7.38 (d, J=7.07 Hz, 1 H) 7.43 (t, J=7.20 Hz, 2 H) 7.46-7.54 (m, 4 H) 7.86-7.94 (m, 2 H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US09149541B2 |
| Source dataset | uspto-grants-2015_10 |
| ORD ID | ord-0ab91288c5e54a28adfd8b49f6c5e448 |
| Source note | uspto-grants-2015_10 |