HuagongsheHuagongshe Chemistry Print Report · For research reference only
Benzyl Isothiocyanate → 4-Benzyl-1-(thiophene-2-carbonyl)thiosemicarbazide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Benzyl Isothiocyanate | HCID 2346 | — |
| Reactant | Thiophene-2-carbohydrazide | HCID 73098 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | 4-Benzyl-1-(thiophene-2-carbonyl)thiosemicarbazide | HCID 5260688 | 89.3% |
Reaction Steps
To a hot solution of 2-thiophencarboxylic acid hydrazide (5.0 g, 35 mmol) in acetonitrile (80 mL) was added neat benzyl isothiocyanate (4.7 mL, 35 mmol) via syringe. When the solvent started to boil, the reaction vessel was removed from the heat source and allowed to cool to room temperature. The resulting crystals were collected by vacuum filtration, washed with diethyl ether and air-dried to yield N-benzyl-2-(thien-2-ylcarbonyl)hydrazinecarbothioamide (9.11 g; 89%; (M+H)+−292.2).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07563905B2 |
| Source dataset | uspto-grants-2009_07 |
| ORD ID | ord-af782016dd43493eba98f290432a7005 |
| Source note | uspto-grants-2009_07 |