HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ethyl bromoacetate → 2-(trans-3-Ethoxycarbonylmethoxystyryl)benzothiazole
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ethyl bromoacetate | HCID 7748 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | HCID 7986269 | HCID 7986269 | — |
| Solvent | Acetone | HCID 180 | — |
| Product | 2-(trans-3-Ethoxycarbonylmethoxystyryl)benzothiazole | HCID 14051175 | 77% |
Reaction Steps
To 30 ml of acetone were added 200 mg of 2-(trans-3-hydroxystyryl)benzothiazole, 0.11 ml of ethyl bromoacetate and 131 mg of potassium carbonate, and the mixture was refluxed for 4 hours. After cooled to room temperature, the mixture was extracted with ethyl ether, dried over anhydrous magnesium sulfate and then the solvent was evaporated under reduced pressure. After the crude crystals of the residue were washed with ethyl ether and n-hexane, they were dried under reduced pressure to give 207 ml (yield 77%) of the title compound.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04902700 |
| Source dataset | uspto-grants-1990_02 |
| ORD ID | ord-33abe700bcb745738dd16b41f5f9c8a4 |
| Source note | uspto-grants-1990_02 |