HuagongsheHuagongshe Chemistry Print Report · For research reference only
Hydrazine → N-aminobenzenecarbothioamide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Hydrazine | HCID 9321 | — |
| Reactant | Methyl 2-((phenylcarbonothioyl)thio)acetate | HCID 71356278 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | N-aminobenzenecarbothioamide | HCID 3361911 | 94% |
Reaction Steps
Add a solution of thiobenzoylsulfanylacetic acid methyl ester (1.9 g, 8.4 mmol) in ethanol (30 mL) to a solution of anhydrous hydrazine (1 mL) at room temperature under nitrogen and stir for 2 hours. Then add water (20 mL) and remove the solvent under reduced pressure. Dissolve the residue in ethyl acetate (300 mL), wash with water (200 mL) and brine (200 mL), and dry over magnesium sulfate. Remove the solvent under reduced pressure to provide thiobenzoic acid hydrazide (1.2 g, 94%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07662771B2 |
| Source dataset | uspto-grants-2010_02 |
| ORD ID | ord-643fe99d9aef4473a01d8af06d2d8ee8 |
| Source note | uspto-grants-2010_02 |