HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ethanol → Ethyl 6,7-dichloro-2,3-dihydro-1-benzofuran-2-carboxylate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ethanol | HCID 702 | — |
| Reactant | Sulfuric Acid | HCID 1118 | — |
| Reactant | 6,7-dichloro-2,3-dihydrobenzofuran-2-carboxylic Acid | HCID 9816065 | — |
| Product | Ethyl 6,7-dichloro-2,3-dihydro-1-benzofuran-2-carboxylate | HCID 12747889 | — |
Reaction Steps
A solution of 6,7-dichloro-2,3-dihydrobenzofuran-2-carboxylic acid (70 g.) conc. sulfuric acid (2 ml.) and ethanol (250 ml.) is refluxed for 2 hours. The ethanol is distilled at reduced pressure and the residue is suspended in saturated sodium bicarbonate and extracted with ether. The ether solution is washed with brine, dried over magnesium sulfate and the ether distilled at reduced pressure. The 6,7-dichloro-2,3-dihydrobenzofuran-2-carboxylic acid ethyl ester is used without further purification in the following synthesis.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04401669 |
| Source dataset | uspto-grants-1983_08 |
| ORD ID | ord-b183a7e0b96b40f69cfc3f16c2fe13d1 |
| Source note | uspto-grants-1983_08 |