Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Water | HCID 962 | — |
| Reactant | HCID 19917017 | HCID 19917017 | — |
| Reactant | HCID 178418260 | HCID 178418260 | — |
| Catalyst | Ferrous Chloride | HCID 24458 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | HCID 19916968 | HCID 19916968 | 44.9% |
Reaction Steps
46 mg of the resulting ether compound was dissolved in 1 ml of dimethylformamide, and 17 mg of copper cyanide was added. The mixture was stirred overnight at 150° C. To this solution was added, a mixture of 39 mg of iron(II) chloride, 0.1 ml of water and 16 μl of hydrochloric acid, and the mixture was stirred at 60° C. for 30 minutes. The solution was extracted with ethyl ether, and the extract was worked up in a customary manner to give 17 mg of 3-[2-[2-(3cyanophenyl)ethoxy]ethyl]thiophene as a colorless oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05439932 |
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| Source dataset | uspto-grants-1995_08 |
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| ORD ID | ord-6e37a3a4aa0e4453b0e0a56025766dad |
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| Source note | uspto-grants-1995_08 |
|---|