HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ethanol → Ethyl 4-hydroxy-3-methoxy-5-nitrophenylglyoxylate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ethanol | HCID 702 | — |
| Reactant | Selenium Dioxide | HCID 24007 | — |
| Reactant | 2-Bromo-4'-hydroxy-3'-methoxy-5'-nitroacetophenone | HCID 14450983 | — |
| Product | Ethyl 4-hydroxy-3-methoxy-5-nitrophenylglyoxylate | HCID 14450984 | — |
Reaction Steps
ba) A suspension of 580.1 mg of 2-bromo-4'-hydroxy-3'-methoxy-5'-nitroacetophenone in 10 ml of ethanol is treated with 443.8 mg of selenium dioxide and heated under reflux for 71 hours. Thereafter, the selenium is removed by filtration and the filtrate is evaporated. The residue is dissolved in methylene chloride, washed with saturated sodium chloride solution, dried over sodium sulfate, filtered and evaporated. There is obtained ethyl 4-hydroxy-3-methoxy-5-nitrophenylglyoxylate of m.p. 165°-167° (from ethanol).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05705703 |
| Source dataset | uspto-grants-1998_01 |
| ORD ID | ord-8f0a0573f6c547bca073b6db73e4d30f |
| Source note | uspto-grants-1998_01 |