HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 126768Generated: October 23, 2026
Boric Acid → Benzo(g)pteridine-2,4(1H,3H)-dione, 7,8-dichloro-
https://huagongshe.com/en/reaction/126768
Participants
| Role | Name | HCID | Charge |
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| Reactant | Boric Acid | HCID 7628 | — |
| Reactant | 2,4,5,6(1H,3H)-Pyrimidinetetrone, monohydrate | HCID 16723 | — |
| Reactant | 4,5-Dichloro-1,2-phenylenediamine | HCID 79297 | — |
| Solvent | Acetic Acid | HCID 176 | — |
| Product | Benzo(g)pteridine-2,4(1H,3H)-dione, 7,8-dichloro- | HCID 5487670 | 99.9% |
Reaction Steps
A solution of 10 g of 4,5-dichloro-o-phenylenediamine, 9 g of alloxan hydrate, 1.5 g of boric acid and 250 ml of glacial acetic acid was stirred overnight at room temperature to obtain a brown-black solution which was filtered. The yellow-buff crystalline solid was well washed with water to obtain 15.9 g of 7,8-dichloro-alloxazine melting at >370° C. A solution of 2 g of 7,8-dichloro-alloxazine in 10 ml of concentrated sulfuric acid was slowly heated to 240° C. and held there for 10 minutes. The mixture was cooled and poured onto ice and the mixture was made alkaline with sodium hydroxide addition. The mixture was extracted several times with ether to obtain 0.73 g of 2-amino-6,7-dichloro-quinoxaline as an orange crystalline solid melting at 220° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04254123 |
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| Source dataset | uspto-grants-1981_03 |
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| ORD ID | ord-fb47faf0040341b8bd2c4fd54bb0c4b5 |
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| Source note | uspto-grants-1981_03 |
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