HuagongsheHuagongshe Chemistry Print Report · For research reference only
Methanol → 4(1H)-Quinazolinone
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Methanol | HCID 887 | — |
| Reactant | Methylorthoformate | HCID 53629101 | — |
| Reactant | 70346-37-1 | HCID 67362646 | — |
| Product | 4(1H)-Quinazolinone | HCID 135408753 | 81% |
Reaction Steps
In a 2-mL volume stainless steel pressure-resistant vessel were placed 280 mg (1.8 mmol) of ammonium anthranilate (prepared in the same manner as in Reference Example 1), 400 mg (3.6 mmol) of methyl orthoformate, and 1.5 mL of methanol. The reaction was carried out at 120° C. for 2 hours. After the reaction was complete, the reaction mixture was cooled to room temperature and analyzed (according to absolute quantitative analysis) by high performance liquid chromatography. There was produced 214 mg (reaction yield: 81%) of quinazolin-4-one.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07232903B2 |
| Source dataset | uspto-grants-2007_06 |
| ORD ID | ord-b2e795dc31064a299c1d4592b82795e1 |
| Source note | uspto-grants-2007_06 |