HuagongsheHuagongshe Chemistry Print Report · For research reference only
Potassium Carbonate → Ethyl (2E)-4-(5-bromo-2-nitrophenoxy)but-2-enoate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | Ethyl (E)-4-bromobut-2-enoate | HCID 5373944 | — |
| Reactant | 5-Bromo-2-nitrophenol | HCID 13970496 | — |
| Solvent | N-methyl-2-pyrrolidone | HCID 13387 | — |
| Product | Ethyl (2E)-4-(5-bromo-2-nitrophenoxy)but-2-enoate | HCID 131736331 | 99% |
Reaction Steps
5-Bromo-2-nitrophenol (10 g, 45.9 mmol) and K2CO3 (8.24 g, 59.6 mmol) were suspended in NMP (81 mL) (a bright red suspension) and ethyl 4-bromocrotonate (10.26 mL, 59.63 mmol) was added dropwise at room temperature. The reaction was stirred at room temperature over night (20 h). The mixture was poured into ice/water (500 mL) and stirred for 30 min. The precipitate was collected by filtration and washed with water (2×200 mL), air dried for 10 min and then washed with heptane (200 mL). Heptane (200 mL) was added to the solid and stirred for 1 h. The solid was filtered off, washed with heptane (2×50 mL) and dried in vacuo to afford a beige solid. The title compound (15.0 g, 99%) was obtained and was used without further purification.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US09394291B2 |
| Source dataset | uspto-grants-2016_07 |
| ORD ID | ord-0fa0ccfe2a234a8e9979fc65f6f0fb09 |
| Source note | uspto-grants-2016_07 |