HuagongsheHuagongshe Chemistry Print Report · For research reference only
Phosgene → 2H-3,1-Benzoxazine-2,4(1H)-dione, 5-nitro-
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Phosgene | HCID 6371 | — |
| Reactant | HCID 70531720 | HCID 70531720 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 2H-3,1-Benzoxazine-2,4(1H)-dione, 5-nitro- | HCID 134795 | — |
Reaction Steps
A solution of 56.5 g of 2-amino-6-nitrobenzoic acid hydrochloride in 200 ml of demineralized water and 200 ml of tetrahydrofuran is cooled to 10° while stirring and treated with phosgene at 10°-30° for 1 hour, a precipitate resulting. The mixture is subsequently diluted with 300 ml of demineralized water and air is conducted through the suspension vigorously for about 3 hours (until the sample is negative for phosgene). The precipitate is filtered off, washed with water and dried in vacuo over phosphorus pentoxide. There is obtained 6-nitroisatoic acid anhydride as beige crystals of m.p. 220°-222° (decomposition).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04386028 |
| Source dataset | uspto-grants-1983_05 |
| ORD ID | ord-e57fd57caacd4ac7a3b0cc650a98fca4 |
| Source note | uspto-grants-1983_05 |