HuagongsheHuagongshe Chemistry Print Report · For research reference only
Dimethylformamide → Ethyl[(6,7-dichloro-2-acetylbenzo[b]thien-5-yl)oxy]acetate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Dimethylformamide | HCID 6228 | — |
| Reactant | Ethyl bromoacetate | HCID 7748 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 2-Acetyl-6,7-dichloro-5-hydroxybenzo[b]thiophene | HCID 13290036 | — |
| Solvent | Methyl Ethyl Ketone | HCID 6569 | — |
| Product | Ethyl[(6,7-dichloro-2-acetylbenzo[b]thien-5-yl)oxy]acetate | HCID 53636860 | 42.6% |
Reaction Steps
To a solution of 9.0 g of 2-acetyl-6,7-dichloro-5-hydroxybenzo[b]thiophene and 200 ml of 2-butanone is added a solution of 6.62 g of ethyl bromoacetate in 50 ml of 2-butanone, 5.2 g of potassium carbonate and 2.2 ml of dimethylformamide. The reaction mixture is heated under reflux for 2 hrs, allowed to cool and filtered. The filtrate is extracted with ether (3 times). The layers are separated and the organic phase is washed with water, saturated sodium chloride solution, dried and filtered. The filtrate is evaporated. The residue is dissolved in dichloromethane and chromatographed on alumina, using dichloromethane as the eluant. Evaporation of the eluant gives 5.1 g of ethyl[(6,7-dichloro-2-acetylbenzo[b]thien-5-yl)oxy]acetate.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04672138 |
| Source dataset | uspto-grants-1987_06 |
| ORD ID | ord-f7025e3bfe8045fd9976145eaa3be22d |
| Source note | uspto-grants-1987_06 |