HuagongsheHuagongshe Chemistry Print Report · For research reference only
Diethyl Sulfate → Ethyl 2-ethoxy-3-(3-nitrophenyl)prop-2-enoate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Diethyl Sulfate | HCID 6163 | — |
| Reactant | Dimethylformamide | HCID 6228 | — |
| Reactant | Cesium carbonate | HCID 10796 | — |
| Reactant | HCID 66905811 | HCID 66905811 | — |
| Product | Ethyl 2-ethoxy-3-(3-nitrophenyl)prop-2-enoate | HCID 66905854 | 72% |
Reaction Steps
Diethyl sulfate (12 g, 78.2 mmol) was added to a stirred mixture of 2-hydroxy-3-(3-nitrophenyl)acrylic acid (6.1 g, 30.0 mmol) and caesium carbonate (29.3 g, 90 mmol) in DMF (61 ml) to form a dear, pale yellow mixture, which was stirred at RT overnight. The resulting dark red suspension was heated to 50° C. for 4 h then concentrated in vacuo and the residue partitioned between water (100 ml) and dichloromethane (150 ml). The organic layer was separated, further washed with water (2×100 ml), dried over sodium sulphate and filtered through a silica gel pad. The resulting yellow solution was evaporated to dryness in vacuo to give ethyl 2-ethoxy-3-(3-nitrophenyl)acrylate as a yellow solid (5.6 g, 72%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US09133099B2 |
| Source dataset | uspto-grants-2015_09 |
| ORD ID | ord-1d0c52fad3824ece962dc336d9819fdc |
| Source note | uspto-grants-2015_09 |