HuagongsheHuagongshe Chemistry Print Report · For research reference only
Methyl iodide → HCID 54713903, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Methyl iodide | HCID 6328 | — |
| Reactant | Allyl bromide | HCID 7841 | — |
| Reactant | HCID 54713869 | HCID 54713869 | — |
| Product | HCID 54713903 | HCID 54713903 | — |
Reaction Steps
In accordance with EXAMPLE 15, using 7-nitro-3-acetoxy-4-hydroxy-1-methyl-2(1H)-quinolinone, allyl bromide was used as an alkylating agent instead of methyl iodide, 7-nitro-3-(2-propenyloxy)-4-hydroxy-1-methyl-2(1H)-quinolinone was provided. In the following, the spectrum data was shown.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05942521 |
| Source dataset | uspto-grants-1999_08 |
| ORD ID | ord-6f75437fe3a14f539da9aa78c67b2acc |
| Source note | uspto-grants-1999_08 |