HuagongsheHuagongshe Chemistry Print Report · For research reference only
Acetone → 1-Benzoyl-2-isopropylhydrazine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Acetone | HCID 180 | — |
| Reactant | Trifluoroacetic acid | HCID 6422 | — |
| Reactant | Benzoylhydrazine | HCID 11955 | — |
| Reactant | Triethylsilane | HCID 12052 | — |
| Solvent | Hexane | HCID 8058 | — |
| Product | 1-Benzoyl-2-isopropylhydrazine | HCID 18869 | 71.1% |
Reaction Steps
A solution of benzoylhydrazine (10 g, 73.45 mmol) in hexane (200 ml) was treated with acetone (54 mL, 734.5 mmol) and refluxed overnight. The precipitate was collected by suction filtration to afford a white solid which was treated with TFA (200 ml) and triethylsilane (24 mL, 149.24 mmol) at 60° C. overnight. The reaction mixture was concentrated under reduced pressure. The residue was partitioned between DCM and 1N NaOH. The organic layer was washed with brine, dried over sodium sulfate, filtered, and concentrated to afford the product as a white solid (9.31 g, 71%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07317125B2 |
| Source dataset | uspto-grants-2008_01 |
| ORD ID | ord-a08399585b7c4b55ac77b1f86320325e |
| Source note | uspto-grants-2008_01 |