HuagongsheHuagongshe Chemistry Print Report · For research reference only
Water → (E)-2-ethyl-1,3-dimethoxy-5-styrylbenzene
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Water | HCID 962 | — |
| Reactant | Iodoethane | HCID 6340 | — |
| Reactant | 2-Bromo-1,3-dimethoxy-5-(2-phenylethenyl)benzene | HCID 66842676 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | (E)-2-ethyl-1,3-dimethoxy-5-styrylbenzene | HCID 66842591 | 70% |
Reaction Conditions
| Temperature | -78 °C |
|---|
Reaction Steps
To a solution of 1-(4-bromo-3,5-dimethoxyphenyl)-2-phenylethene (0.53 g, 1.7 mmol) in THF (10 mL) was added t-Butyl Li (1.1 mL, 1M in THF) at −78° C. After the addition complete, the solution was slowly heated to reflux for 30 min and then cooled down to −78° C. Ethyl iodide (1.2 eq, 0.27 mL) was added to the solution. Water (10 mL) was added after the completion of the reaction. THF was evaporated and the mixture was extracted with CH2Cl2 (3×5 mL). The extract was combined and dried over anhydrous magnesium sulfate. Evaporation of the solution followed by flash chromatography using 20% ether in hexane gave 1,3-dimethoxy-2-ethyl-5-(2-phenylethenyl)benzene in 70% yield.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07321050B2 |
| Source dataset | uspto-grants-2008_01 |
| ORD ID | ord-508c6bb5b95f4087a1273d750501138f |
| Source note | uspto-grants-2008_01 |