HuagongsheHuagongshe Chemistry Print Report · For research reference only
Sodium Chloride → 5-(2-Cyanobutanoyl)thiophene-2-carbohydrazide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Sodium Chloride | HCID 5234 | — |
| Reactant | Potassium Hydroxide | HCID 14797 | — |
| Reactant | Hydrazine hydrate (1:1) | HCID 24654 | — |
| Reactant | Methyl 5-(2-cyanobutanoyl)thiophene-2-carboxylate | HCID 67087195 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | 5-(2-Cyanobutanoyl)thiophene-2-carbohydrazide | HCID 67087378 | — |
Reaction Steps
Methyl 5-(2-cyanobutyryl)thiophene-2-carboxylate (213 mg, 0.90 mmol) in methanol was stirred with 0.1 M potassium hydroxide in methanol (9.0 mL, 0.90 mmol) at room temperature for 10 minutes and then with hydrazine monohydrate (225 mg, 4.50 mg) at 80° C. for 6 hours. After addition of saturated aqueous sodium chloride, the reaction solution was extracted with ethyl acetate, dried over anhydrous magnesium sulfate and concentrated to give the crude desired product.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07968542B2 |
| Source dataset | uspto-grants-2011_06 |
| ORD ID | ord-9b5ebb64dfaa4e4ea0cc52ddc7ad69e1 |
| Source note | uspto-grants-2011_06 |