HuagongsheHuagongshe Chemistry Print Report · For research reference only
Diphosgene → 5-(2-nitrophenyl)-3H-1,3,4-oxadiazol-2-one
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Diphosgene | HCID 10426 | — |
| Reactant | o-Nitrobenzohydrazide | HCID 3781218 | — |
| Solvent | 1,4-Dioxane | HCID 31275 | — |
| Product | 5-(2-nitrophenyl)-3H-1,3,4-oxadiazol-2-one | HCID 312921 | 86.3% |
Reaction Steps
A solution of 2-nitrobenzoylhydrazine (9.05 g, 0.05 mol) in dioxane (30 mL) was slowly added to a solution of trichloromethyl chloroformate (4.6 mL, 0.04 mol) in dioxane (30 mL) at room temperature. On completion of the addition the reaction was heated to reflux for 4 hours. The solvent was evaporated off and the residue re-crystallised from 96% ethanol (50 mL) to give 7.15 g of the 5-(2-nitrophenyl)-3H-[1,3,4]oxadiazol-2-one. M.p. 157-158° C. A solution of the nitro compound (2 g, 9.7 mmol) in 96% ethanol (25 mL) was hydrogenated over 5% palladium on charcoal to give desired 1.6 g of the desired amine.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06696475B2 |
| Source dataset | uspto-grants-2004_02 |
| ORD ID | ord-4d15a7c651b44668922416d2e8a5ce2d |
| Source note | uspto-grants-2004_02 |