HuagongsheHuagongshe Chemistry Print Report · For research reference only
Allyl bromide → Ethyl 2-(3-nitro-4-allyloxyphenyl)propionate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Allyl bromide | HCID 7841 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | Ethyl 2-(4-hydroxy-3-nitrophenyl)propanoate | HCID 21444155 | — |
| Solvent | Acetone | HCID 180 | — |
| Product | Ethyl 2-(3-nitro-4-allyloxyphenyl)propionate | HCID 21444159 | — |
Reaction Steps
A mixture of 2.39g of ethyl 2-(3-nitro-4-hydroxyphenyl)propionate, 1.45g of allylbromide and 1.65g of potassium carbonate in 20ml of acetone was refluxed for 4 hours. After cooling, the solvent was distilled under reduced pressure. The residue was dissolved in ethyl acetate and washed with water. After the solution was dried over magnesium sulfate, the solvent was distilled off. The thus obtained oily substance was purified by means of silica gel chromatography, to give the object compound in a yield of 2.51g (90%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04016193 |
| Source dataset | uspto-grants-1977_04 |
| ORD ID | ord-db37a75043164c6b8b4aa3f1463faeb9 |
| Source note | uspto-grants-1977_04 |