HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1581692Generated: October 25, 2026
Triethylamine → 2,2,2-Triphenylacetohydrazide
https://huagongshe.com/reaction/1581692
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Hydrazine hydrate (1:1) | HCID 24654 | — |
| Reactant | Triphenylacetic acid | HCID 68992 | — |
| Reactant | Tetramethylfluoroformamidinium hexafluorophosphate | HCID 2774761 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | 2,2,2-Triphenylacetohydrazide | HCID 15369986 | 65% |
Reaction Steps
Triphenylacetic acid (499.6 mg, 1.73 mmol) was dissolved in N,N-dimethylformamide (DMF, 3.46 mL). Fluoro-N,N,N′,N′-tetramethylformamidinium hexafluorophosphate (TFFH, 460.1 mg, 1.742 mmol) and anhydrous triethylamine (480 μl, 3.44 mmol) were added and the solution was cooled to 0° C. After 10 minutes hydrazine monohydrate (168 μl, 3.46 mmol) was added. The reaction was allowed to warm, and after stirring at room temperature for 30 minutes, it was worked up by adding water and filtering the resulting precipitate. The precipitate was dried under vacuum to give 2,2,2-triphenylacetohydrazide (340.1 mg).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US06730690B2 |
|---|
| Source dataset | uspto-grants-2004_05 |
|---|
| ORD ID | ord-3f036efc31d04469857c1005108c3b20 |
|---|
| Source note | uspto-grants-2004_05 |
|---|