HuagongsheHuagongshe Chemistry Print Report · For research reference only
Acetone → Acetone diisobutylhydrazone
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Acetone | HCID 180 | — |
| Reactant | Ammonia | HCID 222 | — |
| Reactant | Hydrogen Peroxide | HCID 784 | — |
| Reactant | Acetonitrile | HCID 6342 | — |
| Reactant | Diisobutylamine | HCID 8085 | — |
| Catalyst | Ammonium Acetate | HCID 517165 | — |
| Solvent | Methanol | HCID 887 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Ethylenediaminetetraacetic Acid | HCID 6049 | — |
| Solvent | Disodium | HCID 141233 | — |
| Product | Acetone diisobutylhydrazone | HCID 588027 | 14.1% |
Reaction Steps
A solution was prepared which comprised 206 g diisobutylamine (1.60 mole), 36 g an aqueous solution containing 19.1% by weight NH3 (0.40 mole), 92.6 g acetone (1.60 mole), 41 g acetonitrile (1.00 mole), and 96 g metanol, in which 2.4 g of the disodium salt of ethylenediaminetetracetic acid and 0.4 g ammonium acetate were dissolved. The solution was brought to 50° C, and within the space of half an hour 38.9 g oxygenated water containing 70% by weight H2O2 (0.80 mole) were introduced. The reaction was allowed to continue for seven hours at the same temperature; and the solution was then distilled at 90° C and 20 mm Hg to obtain 26 g acetone N, N-diisobutylhydrazone (0.14 mole, which was 17.5% of the theoretical yield).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US03943132 |
| Source dataset | uspto-grants-1976_03 |
| ORD ID | ord-23c5306e62344caebcc2dbb8390d9117 |
| Source note | uspto-grants-1976_03 |