HuagongsheHuagongshe Chemistry Print Report · For research reference only
Hydrochloric Acid → N-allyl-N'-t-butyl-N,N'-dibenzoylhydrazine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Allyl iodide | HCID 11166 | — |
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | 1,2-Dibenzoyl-1-(tert-butyl)hydrazine | HCID 86307 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | N-allyl-N'-t-butyl-N,N'-dibenzoylhydrazine | HCID 15294608 | — |
Reaction Steps
To a stirred solution of N'-t-butyl-N,N'-dibenzoylhydrazine (3 g, 0.011M) in DMF (30 ml) at room temperature under nitrogen was added portionwise sodium hydride (60% oil dispersion) (0.5 g, 0.012M). The mixture was stirred at room temperature for 0.5 hours, and then allyl iodide (1.8 g, 0.01M) was added dropwise. The reaction mixture was warmed to 60° C. and stirred for 2 hours. The mixture was then diluted with water (50 ml), neutralized with 10% HCl and the product extracted into methylene chloride (50 ml). The methylene chloride layer was washed with water (5×20 ml), dried over anhydrous magnesium sulfate and the methylene chloride removed under vacuum to afford N-allyl-N'-t-butyl-N,N'-dibenzoylhydrazine as an oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05424333 |
| Source dataset | uspto-grants-1995_06 |
| ORD ID | ord-1f565d8e745b4d0f90d3eefa8cd0e70b |
| Source note | uspto-grants-1995_06 |