HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ethyl bromoacetate → HCID 21483949, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ethyl bromoacetate | HCID 7748 | — |
| Reactant | Potassium Hydroxide | HCID 14797 | — |
| Reactant | HCID 21483899 | HCID 21483899 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Solvent | Potassium Carbonate | HCID 11430 | — |
| Product | HCID 21483949 | HCID 21483949 | — |
Reaction Steps
2-Cyclopentyl-6-hydroxy-7,8-dichloro-1-tetralone (9.45 g., 0.03 mole) is heated in a mixture of potassium carbonate (5.52 g.) and ethyl bromoacetate (6.68 g., 0.04 mole) in DMF 70 ml.) at 55°-60° C. for three hours. Potassium hydroxide (2.24 g., 0.04 mole) is added. This solution is added to the reaction mixture and the whole is refluxed for 1 hour. Most of the methanol is evaporated and the residue is added to water (ca. 200 ml.). The solid that separates upon acidification is collected, washed with water and crystallized from ethanol to obtain (1-oxo-2-cyclopentyl-7,8-dichloro-1,2,3,4-tetrahydro-6-naphthyloxy)acetic acid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04003927 |
| Source dataset | uspto-grants-1977_01 |
| ORD ID | ord-bd205683790a4730938c28542b345c06 |
| Source note | uspto-grants-1977_01 |