HuagongsheHuagongshe Chemistry Print Report · For research reference only
Acetic Acid → 1-[2-(2,6-Diethyl-4-methylphenyl)-2-oxoacetyl]-2-(1-methylsulfanyl-2-propylidene)hydrazine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Acetic Acid | HCID 176 | — |
| Reactant | Tetrahydrofuran | HCID 8028 | — |
| Reactant | 1-Methylthio-2-propanone | HCID 6430713 | — |
| Reactant | 2-(2,6-Diethyl-4-methylphenyl)-2-oxoacetohydrazide | HCID 56942873 | — |
| Solvent | Water | HCID 962 | — |
| Product | 1-[2-(2,6-Diethyl-4-methylphenyl)-2-oxoacetyl]-2-(1-methylsulfanyl-2-propylidene)hydrazine | HCID 86689345 | 81.4% |
Reaction Steps
To a 200 ml volume four-necked flask, 2-(2,6-diethyl-4-methylphenyl)-2-oxoacetohydrazine ((12-1)-(11)-39) (6.44 g), tetrahydrofuran (72 ml), and acetic acid (1.65 g) were added under a nitrogen atmosphere. 1-methylsulfanyl-2-propanone (7-0-1) (3.12 g) was added at room temperature, and the mixture was stirred at room temperature for 2 hours. To the reaction mixture was added water (30 ml), and extracted with tert-butyl methyl ether. The organic layer was concentrated under reduced pressure to give 7.17 g of 1-[2-(2,6-diethyl-4-methylphenyl)-2-oxoacetyl]-2-(1-methylsulfanyl-2-propylidene)hydrazine ((4-4)-(8)-39).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08884010B2 |
| Source dataset | uspto-grants-2014_11 |
| ORD ID | ord-f22862d887c94aacbe6b1121c774211b |
| Source note | uspto-grants-2014_11 |