HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ethanol → HCID 178513359, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ethanol | HCID 702 | — |
| Reactant | 2-Thiophenecarbonitrile | HCID 66087 | — |
| Reactant | Hydroxyamine hydrochloride | HCID 443297 | — |
| Reactant | Sodium ethoxide | HCID 2723922 | — |
| Solvent | Cyclohexane pentane | HCID 21949758 | — |
| Product | HCID 178513359 | HCID 178513359 | — |
Reaction Steps
A solution of sodium ethoxide (21% by weight in ethanol, 64.9 ml, 0.174 mol, 1.1 eq.), hydroxylamine hydrochloride (12.1 g, 0.174 mol, 1.1 eq.) and ethanol (100 ml) was refluxed for 30 minutes. Thiophene-2-carbonitrile (18.8 g; 0.172 mol; 1 eq.) was then added and the solution was refluxed continuously for 18 hours. The reaction was monitored by thin layer chromatography (TLC) (50/50 cyclohexane/pentane). The solution was evaporated under reduced pressure and the residue obtained triturated in water at pH 7. The aqueous phase, saturated beforehand with NaCl, was then extracted with ethyl ether (three times). The organic phases were combined, dried over MgSO4 and concentrated under reduced pressure to give a white powder.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08338599B2 |
| Source dataset | uspto-grants-2012_12 |
| ORD ID | ord-11c1277f76704e73836f23feea079440 |
| Source note | uspto-grants-2012_12 |