HuagongsheHuagongshe Chemistry Print Report · For research reference only
Hydroquinone → HCID 18469783, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Hydroquinone | HCID 785 | — |
| Reactant | Potassium Iodide | HCID 4875 | — |
| Reactant | N-Methylformamide | HCID 31254 | — |
| Reactant | HCID 18469781 | HCID 18469781 | — |
| Reactant | Potassium methacrylate | HCID 23667354 | — |
| Product | HCID 18469783 | HCID 18469783 | 92.3% |
Reaction Steps
Next, into a flask of 200 ml capacity fitted with a stirrer and cooling tube, there were introduced 14.9 g of 1-(2-chloroethyl)-4-nitroindole, 18.0 g of potassium methacrylate, 6.0 g of potassium iodide, 40 ml of N, N-methyl formamide and a small quantity of hydroquinone, these then being heated to 100° C., and stirred for 2.5 hours. After the reaction had been completed, insoluble material was removed by filtration, and concentration was performed under reduced pressure. Furthermore, this reaction mixture was purified by column chromatography using silica gel, to obtain 16.8 g of 1-(2-methacryloyloxyethyl)-4-nitroindole.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06416939B1 |
| Source dataset | uspto-grants-2002_07 |
| ORD ID | ord-882e645a037d43899eac45eb1b200b14 |
| Source note | uspto-grants-2002_07 |