Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Ethanol | HCID 702 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | 2-Thiophenecarbonitrile | HCID 66087 | — |
| Reactant | Hydroxyamine hydrochloride | HCID 443297 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 178513359 | HCID 178513359 | 88% |
Reaction Steps
To an ethanol (5 mL) solution of 2-thiophenecarbonitrile (525.5 mg, 5 mmol), 5 M hydroxylamine hydrochloride (1.1 mL) and 1 M sodium hydroxide (5.5 mL) were added. After the reaction mixture was heated at 80° C. for 3 h, water and dichloromethane were added. The organic layer was dried, concentrated and triturated with hexanes to give a white solid 625.8 mg (88%). 1H NMR (DMSO-d6), δ(ppm): 9.6 (s, 1H), 7.46 (m, 2H), 7.05 (t, 1H), 5.93 (bs, 2H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07074809B2 |
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| Source dataset | uspto-grants-2006_07 |
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| ORD ID | ord-a9abdd14d13e4aaab88e0d197f3e87dd |
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| Source note | uspto-grants-2006_07 |
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